COD Research is hiring Aggregate Report Writers for its Pharmacovigilance team in Ahmedabad. The opportunity is suitable for professionals with 1–6 years of experience in aggregate report writing or review and practical knowledge of drug safety reporting.
According to the recruitment information provided, candidates will work on important pharmacovigilance aggregate safety reports, including PSURs, DSURs and PBRERs. The role is particularly relevant for professionals experienced in safety data analysis, regulatory requirements and aggregate safety reporting.
COD Research describes itself as a full-service CRO providing clinical research, clinical trial management and specialized pharmacovigilance services. Its India office is located in Ahmedabad.
COD Research official website
Job Highlights
| Details | Information |
|---|---|
| Company | COD Research Pvt Ltd. |
| Position | Aggregate Report Writer |
| Department | Patient Safety |
| Location | Ahmedabad, Gujarat |
| Experience | 1–6 years |
| Domain | Pharmacovigilance |
| Reports | PSUR, DSUR, PBRER |
| Employment Type | Full-time |
| Posted | September 15, 2026 |
Aggregate Report Writer – Job Responsibilities
The role focuses on aggregate safety reporting and review within pharmacovigilance.
Key responsibilities include:
- Drafting and/or reviewing Periodic Safety Update Reports (PSURs).
- Preparing and reviewing Development Safety Update Reports (DSURs).
- Drafting and reviewing Periodic Benefit-Risk Evaluation Reports (PBRERs).
- Analyzing safety data for aggregate reports.
- Interpreting safety information relevant to periodic reporting.
- Applying applicable regulatory requirements to aggregate safety reports.
- Supporting preparation of high-quality pharmacovigilance documentation.
- Reviewing aggregate reports for accuracy, consistency and completeness.
- Working with patient safety and pharmacovigilance teams.
- Supporting regulatory-compliant aggregate safety reporting activities.
Who Can Apply?
COD Research is looking for professionals with 1–6 years of experience in Aggregate Report Writing and Review within Pharmacovigilance.
Candidates should have experience in one or more of the following:
- PSUR preparation or review
- DSUR preparation or review
- PBRER preparation or review
- Aggregate safety reporting
- Pharmacovigilance
- Safety data analysis
- Regulatory safety reporting
- Benefit-risk evaluation
Professionals with hands-on experience preparing or reviewing periodic safety reports are particularly relevant for this opportunity.
Suitable Educational Background
The supplied recruitment information does not specify a mandatory degree. Candidates from relevant pharmacy, life-science and healthcare backgrounds with the required pharmacovigilance experience may be suitable.
Commonly relevant qualifications include:
B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Life Sciences and other relevant healthcare or pharmaceutical qualifications.
Note: These degrees are suggested based on the nature of the role; they are not stated as mandatory qualifications in the supplied vacancy information.
Key Skills for Aggregate Report Writer Jobs
Candidates targeting Aggregate Report Writer jobs in pharmacovigilance should ideally have knowledge of:
- Aggregate Safety Reporting
- PSUR / PBRER
- DSUR
- Pharmacovigilance
- Safety Data Analysis
- Benefit-Risk Assessment
- Regulatory Reporting
- Drug Safety
- Medical Writing
- Regulatory Guidelines
- Clinical Safety Data
Salary
The supplied COD Research vacancy does not mention an official salary range.
For SEO/schema purposes, a reasonable market estimate for an Aggregate Report Writer with 1–6 years of pharmacovigilance experience in Ahmedabad could be approximately ₹4.5 lakh–₹9 lakh per annum, depending on experience, technical expertise and the employer’s compensation structure.
This is only a market estimate and is not an officially announced COD Research salary.
Why This Opportunity Is Relevant for Pharmacovigilance Professionals
Aggregate safety reporting is an important part of pharmacovigilance because it involves evaluating cumulative safety information and presenting relevant findings in regulatory reports.
Experience with PSURs, DSURs and PBRERs can therefore be valuable for professionals developing careers in:
- Pharmacovigilance
- Drug Safety
- Aggregate Reporting
- Medical Writing
- Regulatory Affairs
- Clinical Safety
- Benefit-Risk Management