Are you looking for exciting Pharmacovigilance jobs in Ahmedabad in 2026? Here is an excellent opportunity for pharmacy graduates and experienced pharmacovigilance professionals! A leading organization is hiring candidates for two important positions: ICSR Data Entry Associate and ICSR Quality Control (QC) Specialist.
The recruitment drive offers opportunities for fresh B.Pharm graduates as well as experienced M.Pharm and Pharm.D professionals. Candidates with knowledge of drug safety, adverse event reporting, ICSR case processing, and pharmacovigilance databases can explore these openings.
The job location is Ahmedabad, Gujarat, with a hybrid working model available. Candidates who can join immediately are preferred.
If you are planning to build your career in drug safety and pharmacovigilance, check the eligibility criteria, required skills, job responsibilities, and application process below.
Pharmacovigilance Recruitment 2026 – Job Highlights
| Particulars | Details |
|---|---|
| Company | Leading Organization |
| Job Domain | Pharmacovigilance / Drug Safety |
| Job Positions | ICSR Data Entry Associate and ICSR QC Specialist |
| Job Location | Ahmedabad, Gujarat |
| Work Model | Hybrid |
| Qualification | B.Pharm, M.Pharm, Pharm.D |
| Experience | Fresher to 2 Years |
| Joining | Immediate Joiners Preferred |
| Application Mode | Online |
| Job Type | Full-Time |
1. ICSR Data Entry Associate – Freshers Can Apply
The ICSR Data Entry Associate position is suitable for fresh pharmacy graduates interested in starting their careers in pharmacovigilance.
This role provides an opportunity to gain practical exposure to Individual Case Safety Report (ICSR) processing and drug safety operations.
Eligibility Criteria
- Educational Qualification: B.Pharm.
- Experience: Freshers to 6 months of experience.
- Candidates should have a basic understanding of pharmacovigilance concepts.
- Good written and verbal communication skills are preferred.
- Knowledge of medical terminology and adverse event reporting is beneficial.
Preferred Technical Skills
Candidates with knowledge or training in the following safety databases may have an advantage:
- Argus Safety
- ARISg
- PV Edge
- Other pharmacovigilance safety databases
Basic knowledge of MedDRA coding, WHO-Drug terminology, and ICSR case processing will also be helpful.
Key Responsibilities
- Receive and register initial and follow-up adverse event reports.
- Perform case triage and duplicate searches.
- Enter patient, medical history, adverse event, and drug information into safety databases.
- Support medical coding using MedDRA and WHO-Drug dictionaries.
- Prepare accurate case narratives based on source documents.
- Maintain data accuracy and follow established pharmacovigilance procedures.
This opportunity is particularly suitable for B.Pharm freshers who want to enter the clinical research and drug safety industry.
2. ICSR Quality Control (QC) Specialist – Experienced Candidates
The ICSR Quality Control Specialist position is designed for pharmacy postgraduates and Pharm.D professionals with hands-on pharmacovigilance experience.
Candidates with experience in ICSR case processing, quality review, safety databases, and regulatory compliance can apply.
Eligibility Criteria
- Educational Qualification: M.Pharm or Pharm.D.
- Experience: 1–2 years of core pharmacovigilance experience.
- Practical experience with global safety databases is required.
- Good understanding of ICSR processing and quality control procedures.
- Knowledge of international pharmacovigilance regulations is preferred.
Required Skills
- Hands-on experience with Argus Safety, ARISg, or similar databases.
- Knowledge of Good Pharmacovigilance Practices (GVP).
- Understanding of GVP Module VI.
- Familiarity with MedDRA coding and medical terminology.
- Experience reviewing case narratives and identifying data discrepancies.
- Strong analytical skills and attention to detail.
Key Responsibilities
- Review processed ICSR cases for accuracy and completeness.
- Identify errors in patient information, adverse events, medical history, and drug details.
- Verify medical coding and case narratives.
- Ensure cases meet applicable quality and regulatory requirements.
- Review case processing timelines and submission readiness.
- Provide feedback to data entry associates to improve quality.
- Support compliance with established pharmacovigilance procedures.
This position is suitable for professionals looking to advance their careers in pharmacovigilance quality assurance and case processing.
Why Build Your Career in Pharmacovigilance?
Pharmacovigilance is an important part of the pharmaceutical and healthcare industry. It focuses on monitoring, assessing, and preventing adverse effects associated with medicines.
With pharmaceutical companies and clinical research organizations supporting global drug safety operations, trained pharmacovigilance professionals can explore several career opportunities.
Some potential career paths include:
- Drug Safety Associate
- ICSR Case Processor
- Pharmacovigilance Quality Analyst
- Pharmacovigilance QC Specialist
- Aggregate Reporting Associate
- Signal Detection Analyst
- Drug Safety Team Lead
Ahmedabad is also an important pharmaceutical and healthcare industry hub, making it a location worth exploring for candidates seeking opportunities in drug safety.
Benefits of This Recruitment Opportunity
1. Opportunities for Freshers
B.Pharm graduates with limited or no experience can apply for the ICSR Data Entry position.
2. Career Growth for Experienced Professionals
M.Pharm and Pharm.D candidates with 1–2 years of experience can explore the ICSR QC opportunity.
3. Hybrid Working Model
The recruitment information mentions a hybrid working arrangement, offering a combination of office-based and work-from-home flexibility. Confirm the exact arrangement with the recruiter.
4. Opportunity to Work in Drug Safety
Candidates can gain exposure to ICSR processing, medical coding, safety databases, and pharmacovigilance quality procedures.
5. Immediate Joining Preference
Candidates available to join immediately may receive preference during the recruitment process.
Important Tips Before Applying
To improve your application, consider the following suggestions:
- Prepare an updated resume highlighting your pharmacy qualification.
- Mention relevant pharmacovigilance training and certifications.
- Include experience with Argus Safety, ARISg, or other safety databases, if applicable.
- Highlight your knowledge of MedDRA and WHO-Drug coding.
- QC applicants should mention their ICSR review experience and GVP knowledge.
- Clearly mention your current location and notice period.
- Ensure that all information submitted in the application form is accurate.
Freshers should focus on their academic knowledge, pharmacovigilance training, medical terminology, and willingness to learn.
How to Apply for Pharmacovigilance Jobs in Ahmedabad?
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Interested and eligible candidates can submit their applications through the online application form provided below.
Application Link:
https://docs.google.com/forms/d/e/1FAIpQLSf0826F8gtUW4uGJwjk-wKAOfUV-Eb5E4bsbDu5DqkMd5ZbsQ/viewform
Important: Review the eligibility criteria carefully before submitting your application. The ICSR Data Entry role is for B.Pharm candidates with fresher to 6 months of experience, whereas the ICSR QC role requires M.Pharm or Pharm.D qualifications and 1–2 years of pharmacovigilance experience.
Note: This recruitment information is based on the opportunity details provided. The employer’s name, salary, exact work schedule, and application deadline have not been specified. Verify these details with the recruiter before proceeding.
Frequently Asked Questions (FAQs)
Q1. Are freshers eligible for Pharmacovigilance jobs in Ahmedabad?
Yes. B.Pharm freshers can apply for the ICSR Data Entry Associate position. Candidates with up to 6 months of experience are also eligible.
Q2. What qualifications are required for ICSR Data Entry jobs?
Candidates must have a Bachelor of Pharmacy (B.Pharm) qualification for the specified Data Entry position.
Q3. What is the eligibility for ICSR QC jobs?
Candidates should have an M.Pharm or Pharm.D qualification with 1–2 years of relevant pharmacovigilance experience.
Q4. Is this a work-from-home opportunity?
The recruitment details mention a hybrid working model. Candidates should confirm the exact work-from-home and office attendance requirements with the recruiter.
Q5. Which safety databases are useful for these positions?
Knowledge of Argus Safety, ARISg, PV Edge, and similar pharmacovigilance databases is beneficial.
Q6. What is ICSR in pharmacovigilance?
ICSR stands for Individual Case Safety Report. It is a report containing information about one or more suspected adverse events associated with a medicinal product in an individual patient.
Q7. How can I apply for these Pharmacovigilance vacancies?
Eligible candidates can apply using the online Google Forms application link provided in this job post.
Final Words
This Pharmacovigilance Hiring Drive 2026 is an opportunity worth exploring for B.Pharm freshers and experienced M.Pharm and Pharm.D professionals.
Whether you are beginning your career in ICSR Data Entry or looking for an experienced QC position, make sure your resume highlights your relevant qualifications, technical knowledge, and pharmacovigilance skills.
Apply through the application link and take the next step towards building your career in pharmacovigilance!
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