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Associate Medical Coder
- Location: Bangalore, India
- Company: Optum
About Job
🎓 Eligibility: Graduate degree in any discipline + Certified Coder (AAPC/AHIMA)
🧪 Experience: 0–1 Year (Freshers Welcome)
💰 Salary: ₹3.2 – ₹4.8 LPA
📝 Job Type: Full-Time | Medical Coding | On-site
🏢 About Optum
Optum, part of UnitedHealth Group, is a global leader in healthcare services, technology, and innovation. With operations in over 150 countries, Optum helps improve patient outcomes and streamline healthcare delivery through data-driven solutions and high-quality medical operations.
📌 Key Responsibilities
✔ Accurately code inpatient/outpatient records using ICD-10 and/or CPT-4 codes.
✔ Maintain 95%+ accuracy in code selection and sequencing.
✔ Abstract and index medical records for statistics and reimbursement purposes.
✔ Meet departmental productivity and coding deadlines.
✔ Attend coding meetings and conferences for skill enhancement.
✅ Eligibility & Skills
✅ Graduate degree in any discipline.
✅ Certified coder – CPC, CCS, CIC, or COC (AAPC/AHIMA).
✅ Strong knowledge of medical terminology, anatomy, and coding guidelines.
✅ Ability to work full-time in a day shift from Bangalore.
🎁 Why Join Optum?
🌐 Work with a leading global healthcare organization.
📈 Career growth in one of the most in-demand healthcare fields.
💼 Competitive salary and skill development opportunities.
🤝 Collaborative and supportive work environment.
Clinical Data Services Associate
- Location: Bangalore, India
- Company: Accenture
About Job
Experience Required: 1–3 years
Qualifications: Bachelor of Pharmacy / Master of Pharmacy
About Accenture
Accenture is a leading global professional services company with expertise in digital, cloud, and security. With 775,000+ employees across 120+ countries, we deliver services in Strategy and Consulting, Technology and Operations, and Accenture Song, powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. At Accenture, we embrace the power of change to create value and shared success for clients, people, shareholders, and communities.
Role Overview
As a Clinical Data Services Associate, you will be aligned with the Life Sciences R&D vertical, supporting clients in clinical trials, regulatory services, pharmacovigilance, and patient solutions. You will play a vital role in clinical data management, ensuring accurate collection, integration, validation, and reporting of clinical trial data to meet regulatory requirements and support product submissions.
Key Responsibilities
* Perform data management activities including discrepancy review, query generation, and query resolution.
* Create CRF Completion Guidelines (CCG) and SAE reconciliation guidelines.
* Identify and raise protocol deviations in clinical databases.
* Conduct edit check validation by creating test cases, writing test scripts, and executing UAT (User Acceptance Testing) for CRF/eCRF databases.
* Support clinical data management projects from start to completion.
* Work with SDTM Mapping (Standard Data Tabulation Model) to ensure structured trial data for regulatory submissions.
* Collaborate with team members to ensure compliance with FDA and other global regulatory requirements.
Required Skills & Competencies
* Strong understanding of Clinical Data Management (CDM) processes.
* Knowledge of SDTM Mapping and regulatory submission requirements.
* Adaptability and flexibility in a dynamic work environment.
* Quick learning ability and attention to detail.
* Ability to work independently within a team-based setup.
Work Environment
* May require working in rotational shifts.
* Individual contributor role with focused responsibilities.
* Interaction primarily with team members and direct supervisor.
Equal Opportunity Statement
Accenture is an equal opportunity employer. All employment decisions are made without regard to race, religion, gender, age, disability, sexual orientation, or any protected category.
✅ Join Accenture and be part of our mission to deliver on the promise of technology and human ingenuity.
Medical Writer - Aggregate Safety Reports
- Location: Bangalore, India
- Company: Indegene
About Job
- End-to-end authoring of safety reports (PBRERs, DSURs, SUSARs).
- Ensure regulatory compliance and submission-readiness.
- Collaborate with teams/clients for document strategy.
- Mentor junior writers.
- Med/Life Sciences degree.
- 2+ yrs in medical writing (safety reports).
- Proficient in safety document authoring.
- Strong regulatory guidelines understanding.
- Full-time in Bangalore.
- Collaborative, remote-ready.
- Global regulatory markets exposure.
- Indegene is an Equal Opportunity Employer.
Medical Writer
- Location: Nagpur, Maharashtra
- Company: Bioexcel Lifesciences & Research LLP
About Job
- Prepare PDE reports per EMA, ICH guidelines.
- Review/analyze toxicology, pharmacology data.
- Conduct literature searches for PDE support.
- Translate complex data into clear reports.
- Collaborate with teams for data accuracy.
- Master’s/PhD in Toxicology, Pharmacology, etc.
- Experience in toxicology report writing (PDE).
- Strong understanding of toxicology principles, guidelines.
- Excellent scientific writing in English.
- Proficiency in literature search tools.
- Analytical mindset for scientific accuracy.
- High integrity with confidential data.
- Commitment to learning.
Regional Medical Advisor
- Location: Bengaluru, Karnataka, India
- Company: Dr. Reddy’s Laboratories Ltd.
About Job
Job Summary:
The Regional Medical Advisor (RMA) will serve as the primary scientific and clinical expert representing Dr. Reddy’s in a designated region. This role focuses on engaging key opinion leaders (KOLs), supporting the execution of medical strategies, and contributing to data generation and scientific exchange within the therapy area.
🎯 Key Responsibilities:
🔬 Scientific Engagement:
Build and maintain peer-level relationships with key thought leaders, physicians, pharmacists, and other healthcare professionals.
Conduct scientific discussions on treatment trends, data, and clinical studies in the assigned therapeutic area (e.g., oncology).
Respond to medical and scientific information requests from healthcare providers.
📊 Medical Affairs Execution:
Assist in the implementation of the Medical Affairs strategic plan, including:
- Medical education
- Product training
- Advisory boards
- Evidence generation projects
- Pre-launch activities
Contribute to data generation via meta-analyses, case studies, and collaborative research.
Publish outcomes in recognized journals and scientific forums.
🧠 Therapy Area Expertise:
Maintain in-depth knowledge of disease trends, treatment patterns, and clinical guidelines.
Collaborate with commercial and strategy teams to translate insights into action plans.
Support internal training of field teams with current scientific data and treatment advancements.
✅ Compliance & Governance:
Ensure strict adherence to Dr. Reddy’s Code of Business Ethics (COBE) and compliance policies.
Oversee the approval of promotional and educational materials in line with compliance timelines.
🌱 Strategic Contributions:
Identify knowledge/practice gaps in the medical community and help bridge them through evidence-based strategies.
Work with therapy area leads to co-develop new product strategies, ideate differentiated solutions, and support new product development.
📚 Qualifications & Skills:
Education:
MBBS with a 2-year full-time postgraduate degree in any medical discipline
OR
MBBS with an MBA from a reputed institution
Experience:
Fresh postgraduate or 0–2 years of experience in Field Medical Affairs
Technical & Functional Skills:
Strong understanding of Oncology (preferred therapy area)
Ability to interpret clinical trials and scientific literature
Understanding of pharma business environment
Scientific acumen and excellent communication skills
Exposure to research methodologies and medical data interpretation
🌍 About the Company:
Dr. Reddy’s Laboratories is a leading multinational pharmaceutical company committed to accelerating access to affordable, innovative medicines. With operations in 66 countries and a workforce of 24,000+, the company focuses on sustainability, innovation, and global healthcare impact.
🎁 Benefits:
Competitive compensation
Relocation and joining support
Medical and life insurance for self and family
Maternity/Paternity benefits
Personalized L&D opportunities
Inclusive and growth-oriented culture
💼 Reporting To: Therapy Area Lead / Medical Affairs Manager
Medical Coding (Fresher)
- Location: Mohali (Work from Office Only)
- Company: Coronis Health
About Job
Coronis Health, Mohali is hiring freshers for Medical Coding. This is a work-from-office opportunity in Mohali.
Location: Mohali (Work from Office Only)
Eligibility: BSc Nursing / B.Pharma / M.Pharma
Shift: Day
Working Culture: 5 days a week
Walk-in Address: C-203, 4th Floor, Phase 8B, Industrial Area, Sector 74, Mohali
Interview Timings: 11:00 AM – 2:00 PM (Monday to Friday)
Walk-in Address: C-203, 4th Floor, Phase 8B, Industrial Area, Sector 74, Mohali Interview Timings: 11.00 AM-2.00 PM (Monday to Friday)
Post Free Job and Hire a Right Candidate - Absolute 0% Brokerage Fee
Nala Genetics - Internship
- Location: Remote
- Company: Nala Genetics
About Job
- Marketing Intern: Assist in event planning, engagement strategies for community events/webinars.
- Legal Intern: Support legal research, contract review, regulatory compliance in health-tech.
- Publications Review Intern: Conduct literature reviews, summarize research findings.
- Bioinformatics Intern: Assist in bioinformatics data analysis, scripting (Python), genomics research.
- Duration: Flexible, typically 3–6 months.
- Work Type: Fully remote.
- Work Culture: Inclusive, innovative, impact-driven.
- Eligibility: Final-year students or recent graduates preferred.
- Why Join: Work on real-world health-tech projects, collaborate internationally, gain hands-on experience.
Clinical Trial Support Associate
- Location: Hydrabad
- Company: Sanofi
About Job
Join Our Team at Sanofi! 🚀
We’re on the lookout for passionate and innovative minds to fill the role of R&D Clinical Trial Support Associate.
Please apply if you are having:
Experience in clinical operations and managing clinical studies is preferred.
Basic knowledge of clinical development, GCP & ICH guidelines, regulations by major regulatory bodies such as FDA (Food and Drug Administration) and EMA (European Medicines Agency), and SOPs/ QDs.
Proficiency in CTMS and financial management experience or ability to quickly learn new systems and processes.
Education: Bachelor’s degree in life sciences, healthcare administration, or related field or equivalent experience
Assist with audit/inspection preparation and contribute to elaborate proper responses to audit/inspections, and provide PAI (Pre-Approval Inspection) readiness admin support.
Prepare CSR appendices, manage BIMO activities,
Audit and inspection administrative activities.
Support access management for any tool/system used for the clinical trial
Monitor CTMS compliance, generate and distribute reports, and oversee system data quality.
Ensure CTMS & Systems Administration tasks
Track budgets at study, country, and site levels, ensuring accurate payment status reporting and effective vendor management in finance systems.
Trainee – Regulatory Affairs
- Location: Not specified (part of Apotex global operations)
- Company: ApoPharma (Apotex Group)
About Job
About the Company
ApoPharma, a member of the Apotex group, is dedicated to discovering, developing, and delivering medicines that improve the quality of life for patients with serious diseases. A key research focus is the pathological role of iron in human disease and developing novel treatments to address it.
Job Summary
As a Trainee in Regulatory Affairs, you will be responsible for collating, compiling, and submitting regulatory documentation for assigned projects, maintaining accurate records in databases, and supporting regulatory projects—particularly tenders. This entry-level role is a great opportunity for fresh graduates to start their career in RA.
Key Responsibilities
Collate, compile, and dispatch regulatory documents to Apotex affiliates/customers.
Ensure timely submission of applications to health authorities and follow up as needed.
Communicate with internal departments for tender submissions and database updates.
Respond to queries from affiliates, customers, and regulatory agencies on submissions.
Maintain and update global regulatory databases, trackers, and status sheets.
Act as backup for team members and support additional projects as assigned.
Complete assigned trainings on time.
Foster teamwork and a collaborative environment in line with company values: Collaboration, Courage, Perseverance, Passion.
Adhere to all compliance programs, quality standards, safety protocols, and HR policies.
Qualifications
Education: B.Pharm / M.Pharm / Pharm.D (fresh graduates encouraged to apply).
Knowledge:
Good academic background.
Understanding of New Product Dossier (NPD) and Product Life Cycle Management (PLCM) submissions is an advantage.
Theoretical understanding of regulatory affairs for International / US / Canada / EU markets.
Skills & Abilities
Strong communication skills.
Attention to detail and accuracy.
Ability to work collaboratively and meet deadlines.
Eagerness to learn regulatory processes and market requirements.
Project Manager – Study Operations
- Location: Remote – India
- Company: Icon
About Job
Position Summary
The Project Manager (Study Operations) is responsible for the planning, execution, monitoring, and delivery of clinical studies within agreed timelines, budget, and quality standards. This role involves cross-functional leadership, oversight of study teams, and ensuring adherence to applicable regulations, guidelines, and client requirements.
Key Responsibilities
1. Study Planning & Start-up
Develop and manage study timelines, budgets, and resource allocation plans.
Collaborate with cross-functional teams (Regulatory, Data Management, Biostatistics, Safety, etc.) to ensure readiness for study start-up.
Ensure all start-up activities comply with ICH-GCP, local regulations, and sponsor requirements.
2. Study Execution & Oversight
Lead study operations from initiation through close-out.
Oversee site selection, activation, and performance.
Monitor study progress, track milestones, and proactively address risks/issues.
Serve as the primary point of contact for sponsors regarding operational aspects.
3. Quality & Compliance
Ensure adherence to study protocols, SOPs, ICH-GCP guidelines, and country-specific regulations.
Maintain inspection readiness and participate in audits/inspections.
4. Leadership & Team Management
Lead, mentor, and motivate study teams to achieve project goals.
Conduct regular team meetings to track deliverables and resolve operational challenges.
Foster collaboration across functional and geographic boundaries.
5. Stakeholder Communication
Prepare and deliver regular project status updates to sponsors and internal management.
Escalate critical risks and propose mitigation strategies.
6. Study Close-out
Ensure timely completion of site close-out activities.
Oversee final data lock, archiving of essential documents, and completion of all contractual obligations.
Qualifications & Experience
Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, or related field.
Minimum 3 years of experience as a Project Manager or Clinical Trial Manager in clinical research.
Proven track record in managing global or regional clinical trials.
Strong knowledge of ICH-GCP, local regulations, and clinical trial lifecycle.
Excellent communication, leadership, and problem-solving skills.
Ability to work independently in a fully remote setting.
Proficiency in project management tools and Microsoft Office Suite.
Key Competencies
Strategic thinking with strong decision-making abilities.
Effective leadership and conflict resolution skills.
High attention to detail and organizational skills.
Ability to manage multiple priorities in a fast-paced environment.
About ICON Strategic Solutions
ICON Strategic Solutions partners with leading global pharmaceutical, biotechnology, and medical device companies to deliver customized clinical development services. Our mission is to improve lives by accelerating the development of new treatments through operational excellence and innovative solutions.
Drug Safety Executive
- Location: Ahmedabad (Office-based)
- Company: Fidelity Health Services
About Job
Position Summary :
The Drug Safety Executive will be responsible for the intake, processing, and management of Individual Case Safety Reports (ICSRs) in compliance with regulatory requirements, company SOPs, and client expectations. The role demands accuracy, attention to detail, and adherence to strict timelines in a fast-paced CRO environment.
Key Responsibilities
Book-in and Data Entry: Perform initial case intake (Book-in) and accurate entry of ICSR data into the safety database.
Data Verification: Review and verify source documents to ensure completeness and correctness of safety data.
Case Processing Support: Assist in case triaging, seriousness and expectedness assessment, and coding using MedDRA.
Timely Reporting: Ensure cases are processed and submitted within regulatory timelines and project deadlines.
Query Management: Communicate with internal teams or clients to obtain missing or clarifying information.
Documentation & Compliance: Maintain accurate records of all activities in line with SOPs, GVP, and global PV regulations.
Collaboration: Work closely with other PV team members to meet quality and productivity targets.
Continuous Improvement: Participate in process improvement initiatives and training programs.
Qualifications & Experience :
Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, or related field.
1–2 years of experience in pharmacovigilance case processing (Book-in & ICSR data entry).
Familiarity with global PV regulations and reporting requirements (FDA, EMA, CDSCO, etc.).
Working knowledge of MedDRA coding and safety database systems (e.g., Argus, ArisG) preferred.
Strong attention to detail, accuracy, and documentation skills.
Good written and verbal communication skills in English.
Ability to work effectively in a team-oriented, deadline-driven environment.
- Key Skills :
ICSR case processing - Book-in & triaging
- MedDRA coding
- Data accuracy & quality checks
- Good communication and interpersonal skills
- Time management & multitasking abilities
Clinical Data Specialist
- Location: Bangalore & Kochi, India
- Company: IQVIA
About Job
Position Summary:
The Clinical Data Specialist provides foundational to intermediate-level data management expertise to support the Clinical Data Management (CDM) team in delivering efficient, high-quality data management outputs that meet client needs. The role may also involve taking on leadership responsibilities for specific data management tasks under the supervision of a Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager.
Key Responsibilities:
Serve as a Data Operations Coordinator (DOC) for:
One protocol with fewer than 5 operational staff, or
15+ easy to moderately complex central laboratory studies.
Lead specific data management tasks (e.g., clinical data coding, database design, testing) with guidance.
Act as a backup to a DOC or DTL when required.
Conduct data review and write/resolve data clarifications.
Lead database audit teams to ensure quality and compliance.
Develop and test databases and edit specifications.
Perform testing of programming outputs.
Ensure adherence to core operating procedures and work instructions.
Maintain effective communication and collaboration within the CDM team.
Qualifications:
Education: Bachelor’s degree in Clinical, Biological, or Mathematical Sciences, or a related field (or equivalent combination of education, training, and experience).
Exposure to medical terminology.
Knowledge of clinical data management processes preferred.
- Key Skills:
Strong attention to detail and accuracy. - Good organizational and problem-solving skills.
- Effective written and verbal communication.
- Ability to work both independently and within a team.
- Familiarity with clinical data systems and tools is an advantage.
Inside Sales Specialist
- Location: Bangalore - Jayanagar
- Company: Clinogenesis Research Institute
About Job
Keyskills : Excellent communication in English, convincing skill, cold calling, Lead conversion, Inside Sales
Industry: Education Management, Career Counselling, EdTech
Responsibilities:
• Identifying and contacting prospective customers through a variety of channels, such as cold
calling, networking, and referrals.
• Creating and putting into practice sales strategies to achieve and exceed revenue goals.
• Keeping up-to-date sales records, reporting on sales indicators, and tracking progress toward
goals.
• Working together with cross-functional teams, such as those for product development and
marketing, to enhance the general sales process and customer experience.
Requirements:
• Bachelor’s degree in business, marketing, or a similar subject is required,
• Strong interpersonal and communication abilities.
• Strong aptitude for planning and time management
• Competent with CRM and Microsoft Office
• Experience in EdTech preferred.
Perks and benefits:
• Performance based incentives
• Indoor work environment
• Paid time off
• Competitive Salary
Interested Candidates Please share the resume to hr@clinogenesis.com
Thanks and Regards,
Sahana
HR – Executive
M: 9972612707
Location – https://g.co/kgs/KBYYgZi
Website – https://clinogenesis.com/
Career Councelor
- Location: Bangalore - Jayanagar
- Company: Clinogenesis Research Institute
About Job
Keyskills : Excellent communication in English, convincing skill, cold calling, Lead conversion, Inside Sales
Industry: Education Management, EdTech
Responsibilities:
• Identifying and contacting prospective customers through a variety of channels, such as cold calling, networking, and referrals.
• Creating and putting into practice sales strategies to achieve and exceed revenue goals.
• Keeping up-to-date sales records, reporting on sales indicators, and tracking progress toward
goals.
• Working together with cross-functional teams, such as those for product development and
marketing, to enhance the general sales process and customer experience.
Requirements:
• Bachelor’s degree in business, marketing, or a similar subject is required,
• Strong interpersonal and communication abilities.
• Strong aptitude for planning and time management
• Competent with CRM and Microsoft Office
• Experience in EdTech preferred.
Perks and benefits:
• Performance based incentives
• Indoor work environment
• Paid time off
• Competitive Salary
Interested Candidates Please share the resume to hr@clinogenesis.com
Thanks and Regards,
Sahana
HR – Executive
M: 9972612707
Location – https://g.co/kgs/KBYYgZi
Website – https://clinogenesis.com/
Medical Data Abstractor
- Location: Airoli, Navi Mumbai (Work from Office)
- Company: Omega Healthcare Management Services
About Job
Work Timings: Monday to Friday, 9:00 AM – 6:00 PM (Saturday & Sunday off)
Position Overview
Omega Healthcare is seeking passionate and detail-oriented Medical Data Abstractors to join our growing team. In this role, you will be responsible for accurately abstracting, reviewing, and validating patient medical records and clinical data to support high-quality healthcare documentation, reporting, and decision-making.
Key Responsibilities
* Review, extract, and abstract clinical and non-clinical data from medical records, patient charts, and healthcare documents.
* Ensure accuracy, consistency, and completeness of abstracted data in line with organizational standards.
* Maintain up-to-date knowledge of medical terminology, coding standards, and healthcare documentation practices.
* Work collaboratively with internal teams to resolve discrepancies or clarify missing information.
* Meet project deadlines while maintaining a high standard of quality and compliance.
* Safeguard patient confidentiality and comply with HIPAA and other healthcare regulations.
Required Qualifications
* Graduate or Postgraduate in Medical/Healthcare stream:
* BDS, MDS, BAMS, BUMS, BHMS, BPT, MD, Pharm D
* 0–5 years of experience in clinical or non-clinical settings.
* Strong knowledge of medical terminologies and healthcare documentation.
* Excellent attention to detail and ability to work with large sets of medical data.
* Ability to work independently, prioritize tasks, and meet deadlines.
Desired Skills
* Prior experience in medical data abstraction, coding, or clinical documentation (preferred but not mandatory).
* Strong written and verbal communication skills.
* Proficiency in MS Office tools (Excel, Word, Outlook).
Why Join Us?
* Opportunity to work with one of the leading healthcare management service providers.
* A supportive, growth-driven work environment.
* Competitive salary with fixed day shift and weekends off.
Clinical Evaluation Medical Writer
- Location: Mumbai (Remote)
- Company: Medtronic
About Job
About Medtronic
Medtronic is a global healthcare technology leader, driven by a mission to alleviate pain, restore health, and extend life. With 95,000+ employees worldwide, we are committed to innovation and healthcare access, empowering people to live healthier lives.
Role Overview
As a Clinical Evaluation Medical Writer, you will be responsible for preparing, reviewing, and maintaining clinical evaluation documents in alignment with regulatory requirements. This role involves literature review, data analysis, and preparation of scientific content to support submissions, audits, and product lifecycle management.
Key Responsibilities
* Conduct and summarize comprehensive literature reviews from peer-reviewed sources.
* Critically appraise, analyze, and discuss clinical evidence for medical devices.
* Maintain and update clinical evidence databases and documentation.
* Prepare Clinical Evaluation Plans (CEPs) and Clinical Evaluation Reports (CERs) as per EU MDR / MEDDEV guidelines.
* Generate and maintain state-of-the-art reports for product families.
* Provide scientific support for regulatory submissions, audits, and compliance queries.
* Collaborate with cross-functional teams (Regulatory, Quality, R&D) to ensure alignment.
* Review and approve related product documentation for compliance and accuracy.
* Ensure all writing is consistent with FDA, EMA, ICH, and GCP guidelines.
* Mentor or provide guidance to junior professionals, when required.
Required Qualifications
* Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field.
* Minimum 2 years of relevant medical writing / regulatory writing experience (or Master’s degree with 0–1 year experience).
* Strong knowledge of clinical evaluation requirements for medical devices (EU MDR, MEDDEV 2.7/1 Rev. 4).
* Ability to critically review clinical literature and summarize complex scientific data.
* Excellent written and verbal English communication skills.
* Proficiency in MS Office and literature search databases (e.g., PubMed, Embase).
Preferred Skills & Competencies
* Experience in regulatory writing for medical devices.
* Knowledge of clinical trial processes and regulatory submissions.
* Strong analytical, problem-solving, and project management skills.
* Ability to work independently with minimal supervision.
* Detail-oriented with high-quality documentation standards.
Why Join Medtronic?
* Competitive salary and flexible benefits package.
* Opportunity to work remotely with a global team.
* Be part of a mission-driven company focused on innovation and impact.
* Career development through continuous learning and exposure to cutting-edge medical technologies.
Clinical Trial Coordinator
- Location: Hyderabad
- Company: I’SHNOVA CLINICALS
About Job
Work Timings: Monday to Friday, 9:00 AM – 6:00 PM (Saturday & Sunday off)
Position Overview
Omega Healthcare is seeking passionate and detail-oriented Medical Data Abstractors to join our growing team. In this role, you will be responsible for accurately abstracting, reviewing, and validating patient medical records and clinical data to support high-quality healthcare documentation, reporting, and decision-making.
Key Responsibilities
* Review, extract, and abstract clinical and non-clinical data from medical records, patient charts, and healthcare documents.
* Ensure accuracy, consistency, and completeness of abstracted data in line with organizational standards.
* Maintain up-to-date knowledge of medical terminology, coding standards, and healthcare documentation practices.
* Work collaboratively with internal teams to resolve discrepancies or clarify missing information.
* Meet project deadlines while maintaining a high standard of quality and compliance.
* Safeguard patient confidentiality and comply with HIPAA and other healthcare regulations.
Required Qualifications
* Graduate or Postgraduate in Medical/Healthcare stream:
* BDS, MDS, BAMS, BUMS, BHMS, BPT, MD, Pharm D
* 0–5 years of experience in clinical or non-clinical settings.
* Strong knowledge of medical terminologies and healthcare documentation.
* Excellent attention to detail and ability to work with large sets of medical data.
* Ability to work independently, prioritize tasks, and meet deadlines.
Desired Skills
* Prior experience in medical data abstraction, coding, or clinical documentation (preferred but not mandatory).
* Strong written and verbal communication skills.
* Proficiency in MS Office tools (Excel, Word, Outlook).
Why Join Us?
* Opportunity to work with one of the leading healthcare management service providers.
* A supportive, growth-driven work environment.
* Competitive salary with fixed day shift and weekends off.
Clinical Data Associate
- Location: Bengaluru
- Company: Thermo Fisher Scientific
About Job
Work Schedule: Second Shift (1:00 PM – 10:00 PM IST)
Work Mode: Office / Remote / Hybrid
Environment: Adherence to Good Manufacturing Practices (GMP) and Safety Standards
Role Overview
As a Clinical Data Associate II (CDA), you will play a pivotal role in supporting global data management projects within clinical research. You will ensure the accuracy, consistency, and integrity of clinical trial data while complying with Good Clinical Practices (GCPs), SOPs/WPDs, and client requirements. This position requires advanced problem-solving skills, strong attention to detail, and the ability to collaborate effectively with global teams.
Key Responsibilities
* Identify, resolve, and update data discrepancies in the clinical data management database.
* Generate, track, and resolve data clarifications and queries.
* Review Case Report Forms (CRFs) and support CRF design when required.
* Analyze data listings for accuracy and consistency; resolve data validation issues.
* Produce status reports for CDM management and clients.
* Perform SAE (Serious Adverse Event) and third-party vendor reconciliations.
* Execute advanced aspects of the data cleaning process with high accuracy.
* Ensure compliance with GCP, SOPs, and WPDs during all data management activities.
* Contribute to the development of processes, concepts, and techniques within data management.
* Independently determine methods and procedures for new assignments.
* Collaborate with internal stakeholders and external organizations with professionalism and tact.
Education & Experience
* Bachelor’s degree or equivalent in Life Sciences or related field.
* Minimum 2+ years of experience in Clinical Data Management or related field.
* Equivalent combination of education, training, and experience may also be considered.
Knowledge, Skills & Abilities
* Strong understanding of clinical data management processes and regulatory requirements.
* Experience with EDC systems such as Medidata Rave and Veeva Vault.
* Knowledge of eTMF practices and clinical trial documentation.
* Excellent attention to detail, analytical ability, and problem-solving skills.
* Proficiency in Microsoft Office applications and comfort with interactive computer systems.
* Effective written and verbal communication skills in English.
* Strong time management, organizational skills, and ability to meet deadlines.
* Experience working with global teams, demonstrating cultural awareness and customer focus.
* Ability to maintain confidentiality with sensitive data.
* Knowledge of clinical/medical terminology, protocols, and Data Validation Manual (DVM).
* Flexible, adaptable, and capable of working independently or within a team
Process Excellence Coordinator
- Location: Bengaluru
- Company: Labcorp
About Job
Employment Type: Full-Time
About the Role
Labcorp is seeking a Process Excellence Coordinator (Certified Green Belt or equivalent) to drive Continuous Improvement initiatives locally, ensure alignment with global Process Excellence standards, and partner with cross-functional teams to deliver impactful business outcomes.
Key Responsibilities
* Lead process improvement projects, ensuring timely completion aligned with business goals and customer satisfaction.
* Act as the departmental point of contact for project initiatives and best practices.
* Collaborate across Labcorp functions with process owners, champions, and leaders to set priorities, design objectives, and facilitate Process Excellence activities.
* Train and coach team members and stakeholders on problem-solving, Lean, and process design tools.
* Develop and present business cases supporting changes to existing practices; monitor progress of implementations.
* Partner with different organizational levels to enhance productivity, employee engagement, customer satisfaction, and business growth.
* Demonstrate strong project management skills: planning, execution, resource optimization, and managing competing priorities.
Experience & Skills Required
* 3–5 years of experience in a technical role with exposure to process improvement.
* Certified Green Belt (or equivalent) with hands-on Process Excellence experience.
* Strong quantitative reasoning; ability to analyze and interpret data.
* Proficiency in MS Office (Word, Excel, PowerPoint), Visio, Minitab, and other statistical tools.
* Excellent communication skills (oral and written), with ability to influence and engage stakeholders.
* Strong leadership, problem-solving, and adaptability in dynamic environments.
* Ability to train others in Problem Solving, Lean, and Project Management fundamentals.
Education
* Minimum Bachelor’s degree (BS/BA) in Science, Arts, or related field.
People Interaction
* No direct reports; however, requires regular collaboration with internal teams, Process Excellence leads, functional leaders, and clients.
Why Join Labcorp?
Labcorp is an equal opportunity employer committed to fostering diversity, inclusion, and belonging. We provide a collaborative environment to grow professionally while contributing to innovations that improve lives globally.
Project Coordinator (Core Laboratory)
- Location: Navi Mumbai, India (Office-based)
- Company: Medpace
About Job
About Medpace
Medpace is a full-service Clinical Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device industries. With headquarters in Cincinnati, Ohio, and operations across 40+ countries, Medpace leverages its regulatory and therapeutic expertise to accelerate the global development of safe and effective medical therapeutics.
Role Overview
As a Project Coordinator in the Core Laboratory division, you will support the management of imaging studies within clinical trials. The role involves coordinating project timelines, reporting, maintaining inventory for study sites, and liaising with both internal teams and external study sites. This entry-to-mid-level role is ideal for candidates with strong organizational, communication, and technical skills, looking to build a career in clinical research project management.
Key Responsibilities
* Compile and maintain project-specific status reports and study timelines for imaging studies.
* Track and manage inventory of imaging supplies for clinical trial sites.
* Coordinate with clinical trial sites and internal teams to ensure smooth study execution.
* Assist project managers with operational tasks related to study setup, maintenance, and close-out.
* Ensure documentation accuracy and compliance with study protocols, SOPs, and regulatory standards.
* Contribute to cross-functional collaboration between Core Labs, Project Management, and other stakeholders.
Qualifications
Education:
* Bachelor’s Degree (required) in Biomedical Engineering, Life Sciences, or related field.
* Master’s / PhD in Biomedical Engineering or related discipline (preferred).
Experience:
* Prior research-related or project coordination experience (preferred).
* Exposure to clinical research, imaging studies, or CRO environment will be an advantage.
Skills:
* Excellent organizational, time management, and multitasking skills.
* Strong written and verbal communication abilities.
* Proficiency in MS Office and database tools.
* Detail-oriented, with the ability to work collaboratively in a fast-paced environment.
Why Join Medpace?
* Competitive compensation and benefits package.
* Flexible work environment with wellness and employee appreciation initiatives.
* Generous PTO (Paid Time Off) and structured career paths for growth.
* Opportunities to work on global projects across therapeutic areas such as oncology, cardiology, metabolic disease, CNS, anti-viral, and infectious diseases.
* Recognized as one of America’s Most Successful Midsize Companies by Forbes (2021–2024) and recipient of multiple CRO Leadership Awards.
Clinical Research Coordinator (CRC)
- Location: Belagavi, Karnataka
- Company: Shree Clinical Research Services Pvt. Ltd.
About Job
Department: Clinical Operations
Experience: Freshers / Experienced (as per project requirements)
Education: B.Sc / M.Sc (Life Sciences, Nursing, Pharmacy, or related field)
Position Overview
The Clinical Research Coordinator (CRC) will be responsible for supporting and coordinating clinical trial activities at the study site. The role ensures compliance with study protocols, ICH-GCP guidelines, regulatory requirements, and sponsor/CRO SOPs while maintaining high-quality data collection and patient safety.
Key Responsibilities
* Assist the Principal Investigator (PI) in the planning, initiation, execution, and close-out of clinical trials.
* Screen, recruit, and enroll study participants as per inclusion/exclusion criteria.
* Coordinate informed consent process ensuring patient understanding and documentation.
* Maintain and update source documents, Case Report Forms (CRFs/eCRFs), and essential documents in Trial Master File (TMF/ISF).
* Manage study visits, patient follow-ups, and sample collection/processing as per protocol.
* Ensure protocol adherence and timely reporting of protocol deviations and adverse events (AEs/SAEs).
* Coordinate with sponsors/CROs, monitors, and regulatory authorities during site monitoring visits and audits.
* Maintain accurate investigator site files (ISF) and ensure readiness for inspection.
* Support in preparation and submission of regulatory/ethics committee documents.
* Ensure strict compliance with ICH-GCP guidelines, SOPs, and site policies.
Requirements
* Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, or related discipline.
* Prior experience as CRC in clinical trials (preferred, but freshers with strong interest may be considered).
* Good knowledge of ICH-GCP guidelines and regulatory requirements.
* Strong organizational and documentation skills.
* Excellent communication and interpersonal abilities to coordinate with patients, investigators, and sponsors.
* Ability to handle multiple tasks and meet project deadlines.
Why Join Us?
* Opportunity to gain hands-on experience in clinical trial operations.
* Exposure to multicentric clinical studies and sponsor collaborations.
* Structured learning under guidance of experienced investigators.
* Growth opportunities in Clinical Research & Site Management.
Safety Analyst / Safety Writing Specialist
- Location: Pune, India
- Company: EVERSANA
About Job
Experience: 0–4 years
Qualification: Degree in Pharmacy / Life Sciences
Employment Type: Full-time
Role Overview
The Safety Analyst / Safety Writing Specialist will support pharmacovigilance operations by analyzing safety data, authoring safety reports, and ensuring regulatory compliance. The role offers exposure to both safety case processing and aggregate safety writing, providing opportunities for growth in drug safety and medical writing domains.
Key Responsibilities
* Perform collection, review, and processing of adverse event (AE) and serious adverse event (SAE) cases from clinical trials and post-marketing surveillance.
* Maintain compliance with global pharmacovigilance regulations and company SOPs.
* Assist in the preparation of aggregate safety reports including PADERs, DSURs, PSURs/PBRERs, and other periodic safety updates.
* Support signal detection and risk management activities under the guidance of senior safety experts.
* Author and QC safety-related documents such as line listings, case narratives, and safety data summaries.
* Collaborate with cross-functional teams (PV Scientists, Medical Writers, QA, Regulatory Affairs).
* Participate in audits, inspections, and contribute to CAPA implementation.
* Ensure timely completion and quality compliance of all deliverables.
Requirements
* Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, Nursing, or related fields.
* 0–4 years of relevant experience in Pharmacovigilance / Drug Safety / Safety Writing.
* Knowledge of ICH-GCP, pharmacovigilance guidelines, MedDRA, and safety databases (e.g., Argus, ARISg) preferred.
* Strong analytical, documentation, and communication skills.
* Ability to manage multiple deliverables and work in a team-oriented environment.
Why EVERSANA?
* Work with a global leader in life sciences services.
* Exposure to both safety operations and aggregate writing projects.
* Learning opportunities under experienced PV and safety writing professionals.
* Growth-focused culture with career progression pathways.
Clinical Research Associate (CRA)
- Location: Bhubaneswar, Odisha
- Company: Indivirtus Global CRO Pvt. Ltd.
About Job
Experience: 2–3 years as CRA or Research Associate
Department: Clinical Operations
Employment Type: Full-time
Role Overview
The Clinical Research Associate (CRA) will play a key role in clinical trial execution by managing site activities, ensuring data integrity, regulatory compliance, and maintaining effective site relationships. The CRA will collaborate closely with investigators, sites, and project teams to achieve high-quality trial delivery.
Key Responsibilities
* Conduct site identification, feasibility, and selection activities.
* Oversee and manage clinical monitoring activities to ensure compliance with protocols, SOPs, ICH-GCP, and applicable regulatory requirements.
* Perform site initiation, monitoring, and close-out visits.
* Ensure accurate site documentation, source data verification (SDV), data collection, and drug accountability.
* Collate and review regulatory documentation from investigator sites.
* Proactively manage site performance and resolve site-related issues.
* Complete routine administrative and reporting tasks in a timely and accurate manner.
* Collaborate with project teams to ensure seamless trial conduct.
* Maintain effective communication with investigators and site staff.
Qualifications & Skills
* Bachelor’s/Master’s degree in Life Sciences / Pharmacy / Nursing or related field.
* 2–3 years of experience in clinical research as CRA or RA.
* Strong knowledge of ICH-GCP, clinical trial regulations, and site management practices.
* Excellent interpersonal, communication, and presentation skills.
* Ability to multi-task, prioritize, and work independently or in a team.
* Flexible to travel (including overnight and occasional weekend travel).
* Client-focused mindset with attention to detail.
Why Join Indivirtus Global CRO?
* Be part of a fast-growing CRO with diverse project exposure.
* Opportunity to work in a dynamic and supportive team environment.
* Gain hands-on experience with clinical operations and site management.
* Career growth opportunities with continuous learning.
* Make a direct impact in advancing healthcare and clinical research.
Data Entry Intern
- Location: Bangalore (On-site)
- Company: Portea
About Job
Position: Data Entry Internship
Stipend/Duration: As per company norms
About the Role
As a Data Entry Intern at Portea, you will gain hands-on experience in managing, organizing, and analyzing company data. This role will provide exposure to practical data management processes using MS-Excel and MS-Office, helping you build strong analytical and organizational skills in a dynamic healthcare environment.
Key Responsibilities
* Input, update, and maintain large volumes of data in databases and spreadsheets.
* Perform regular data quality checks to ensure accuracy and completeness.
* Assist in basic data analysis and preparation of reports for management review.
* Collaborate with team members to streamline data processes and improve efficiency.
* Identify and resolve data discrepancies or inconsistencies in records.
* Participate in training sessions to enhance technical and data management skills.
* Ensure confidentiality and security of sensitive information while following best practices.
Desired Skills & Qualifications
* Proficiency in MS-Excel and MS-Office.
* Strong attention to detail and accuracy.
* Good organizational and time-management skills.
* Ability to work independently as well as in a team.
* Enthusiasm to learn and apply data management concepts.
About the Company
Portea is India’s leading provider of home healthcare, delivering quality care through experienced doctors, nurses, and advanced medical infrastructure—right at the patient’s doorstep. Portea is committed to making healthcare more accessible, accountable, and affordable across the country.
Pharmacovigilance Associate
- Location: Pune (Work from Office)
- Company: Wipro Ltd.
About Job
Experience: 1–2 years
Qualification: Pharmacy Graduate with Valid Pharmacy License
About Wipro
Wipro is a leading global information technology, consulting, and business process services company. With innovation-driven solutions, Wipro partners with clients across industries, including pharmaceutical and healthcare, to enhance compliance, patient safety, and operational excellence.
Role Overview
As a Pharmacovigilance Associate, you will play a critical role in monitoring, assessing, and reporting adverse drug reactions (ADRs) to ensure patient safety and regulatory compliance. You will work within global pharmacovigilance systems, adhering to regulatory guidelines and client-specific requirements.
Key Responsibilities
* Perform case processing of adverse events (AEs) and serious adverse events (SAEs) in compliance with regulatory and client requirements.
* Review, code, and validate safety data using MedDRA and WHO-DD.
* Conduct literature screening and review for safety signals and case identification.
* Prepare narratives, case summaries, and regulatory reports (ICSRs, PSURs, DSURs, etc.).
* Ensure timely case entry, data quality, and regulatory submissions.
* Support signal detection, aggregate report preparation, and risk management activities.
* Collaborate with medical reviewers, quality teams, and regulatory authorities as needed.
* Maintain up-to-date knowledge of global PV regulations (ICH, EMA, FDA, CDSCO, etc.).
Skills & Competencies
* Strong knowledge of pharmacovigilance processes and regulatory requirements.
* Hands-on experience with safety databases (e.g., Argus, ARISg, or equivalent).
* Good understanding of drug safety terminology (MedDRA, WHO-DD coding).
* Excellent analytical, problem-solving, and attention-to-detail skills.
* Strong written and verbal communication skills.
* Ability to work in fast-paced, regulated environments.
Why Join Wipro?
* Opportunity to work with global pharmaceutical clients.
* Exposure to end-to-end pharmacovigilance lifecycle.
* Strong focus on career growth and skill enhancement.
* Supportive workplace fostering learning, compliance, and innovation.
Walk-in Interview Details
📅 Date: 4th September 2025
🕒 Time: 11:00 AM
📍 Venue: Wipro, Hinjewadi Phase 2, Rajiv Gandhi Infotech Park, Pune
Business Advisory New Associate
- Location: Bangalore
- Company: Accenture
About Job
Experience: 0–1 year
Qualification: Any Graduation
About Accenture
Accenture is a global professional services leader with expertise in digital, cloud, and security. With 775,000+ professionals worldwide, we deliver innovative solutions in Strategy & Consulting, Technology, Operations, and Accenture Song across 120+ countries. We embrace diversity, inclusion, and well-being to help our people and clients thrive.
Role Overview
As a Business Advisory New Associate – Trust & Safety (AML), you will be part of a team ensuring a safe and compliant digital ecosystem. Your role involves reviewing user-generated content, investigating suspicious activities, and supporting anti-money laundering (AML) compliance by applying KYC rules, AML laws, and client policies. This role demands attention to detail, emotional resilience, and critical thinking skills, as you may be exposed to sensitive content.
Key Responsibilities
* Analyze, review, and classify user profiles, text, audio, and video content per client guidelines.
* Investigate and resolve AML-related issues, escalating complex cases to the Trust & Safety team.
* Understand, implement, and stay updated on AML laws, KYC regulations, and client compliance programs.
* Perform content moderation to ensure platform safety, objectivity, and adherence to client standards.
* Document findings, prepare reports, and support compliance audits.
* Collaborate with team members while working under supervision in a structured process.
* Adhere to rotational shifts and contribute as an individual team contributor.
What We’re Looking For
* Strong coping and emotional resilience to handle objectionable/sensitive content.
* Excellent comprehension, written and verbal communication skills.
* Detail-oriented with analytical, critical thinking, and decision-making ability.
* Ability to synthesize information from multiple sources.
* Objectivity in applying client policies, free from personal bias.
* Flexibility to work in rotational shifts.
Why Join Accenture?
* Work at the forefront of Trust & Safety and AML compliance.
* Access to continuous learning, certifications, and career development.
* Strong focus on employee well-being, diversity, and inclusion.
* Be part of a global team driving innovation and positive impact.