Veeda Lifesciences is currently hiring a Medical Coder – Pharmacovigilance for professionals with 2–4 years of experience in medical coding, MedDRA terminology, and ATC coding within the pharmaceutical or clinical research industry.
This remote pharmacovigilance job offers an excellent opportunity for candidates working in clinical data management, safety data processing, and adverse event coding. The selected candidate will support medical coding activities in clinical trials and pharmacovigilance projects, ensuring that medical terms related to adverse events (AEs), medical history, and drug-related conditions are coded accurately using standardized medical dictionaries such as MedDRA and ATC classification systems.
Medical coding professionals play a critical role in clinical data standardization, safety signal detection, and regulatory reporting in global clinical trials and pharmacovigilance programs.
Job Details
| Parameter | Details |
|---|---|
| Job Title | Medical Coder – Pharmacovigilance |
| Company | Veeda Lifesciences |
| Job Type | Full-time |
| Work Mode | Remote |
| Experience | 2–4 Years |
| Department | Pharmacovigilance / Clinical Data Management |
| Key Skills | MedDRA Coding, ATC Coding, EDC Systems |
Key Responsibilities – Medical Coding in Pharmacovigilance
The Medical Coder – Pharmacovigilance will be responsible for executing medical coding activities across clinical studies and ensuring standardized terminology usage for safety reporting.
Medical Coding Activities
- Perform MedDRA coding for adverse events (AEs), medical history, and medical conditions.
- Apply ATC classification coding for drug-related data.
- Ensure coding activities follow approved medical dictionaries and sponsor guidelines.
- Maintain coding consistency across clinical study databases.
Data Management & Clinical Study Support
- Collaborate with clinical data managers, pharmacovigilance teams, and clinical scientists.
- Raise queries within eCRF systems or EDC platforms regarding coding discrepancies.
- Review sponsor comments and finalize coded terms accordingly.
Reporting & Documentation
- Prepare medical coding reports and performance metrics.
- Track backlog and ensure coding tasks are completed within agreed timelines.
- Maintain documentation aligned with clinical data management standards and SOPs.
Training & Collaboration
- Develop training materials related to medical coding activities.
- Conduct on-the-job training for new hires.
- Participate in departmental meetings to improve coding processes and best practices.
Required Skills and Qualifications
Candidates applying for this medical coder pharmacovigilance job should meet the following criteria:
Educational Qualification
- B.Pharm, M.Pharm, Pharm.D, Life Sciences, or related healthcare degree.
Professional Experience
- 2–4 years of experience in medical coding within pharma or CRO industry.
- Experience working with clinical data management and pharmacovigilance operations.
Mandatory Skills
- MedDRA Coding
- ATC Coding
Preferred Technical Skills
- Experience with EDC systems such as Medidata Rave, Oracle Inform, or similar platforms.
- Knowledge of clinical data management processes including database development and closeout activities.
- Basic knowledge of programming or data management tools.
Why Join Veeda Lifesciences?
Working with Veeda Lifesciences pharmacovigilance and clinical research teams provides exposure to global clinical trial operations and regulatory-compliant medical coding practices.
Benefits of This Role
- Remote working opportunity
- Exposure to global clinical research projects
- Experience with advanced clinical data management systems
- Career growth in pharmacovigilance and medical coding
How to Apply
Interested candidates can apply for this Medical Coder – Pharmacovigilance job at Veeda Lifesciences by sending their updated CV to:
📧 mahendra.t3705@veedalifesciences.com
Applicants with experience in MedDRA coding, ATC classification, pharmacovigilance data management, and clinical trial coding activities are strongly encouraged to apply.
