Introduction
If you are building your career in Pharmacovigilance and Drug Safety, this opportunity from Apcer Life Sciences can be a strong next step. Apcer Life Sciences, a globally recognized life sciences and pharmacovigilance services organization, is currently hiring Pharmacovigilance Associates for its Ahmedabad, Gujarat location.
This role is ideal for professionals with 2–5 years of hands-on experience in ICSR processing, safety data entry, medical coding, and PV compliance who want long-term growth in global drug safety operations.
About Apcer Life Sciences
Apcer Life Sciences is a leading global provider of pharmacovigilance, regulatory affairs, medical writing, and clinical research services.
The company supports pharmaceutical, biotechnology, and medical device companies across the entire product lifecycle, from clinical development to post-marketing safety surveillance.
Company Details
- Company Name: Apcer Life Sciences
- Headquarters: Ahmedabad, Gujarat, India
- Founded: 2010
- Global Presence: India, USA, Europe
- Employees: 1,500+ professionals worldwide
- Core Services: Pharmacovigilance, Drug Safety, Regulatory Affairs, Medical Writing, Clinical Research
Apcer is known for its quality-driven culture, regulatory compliance, and global PV project exposure, making it a preferred organization for drug safety professionals.
Job Overview Summary
Apcer Life Sciences is hiring Pharmacovigilance Associates to support end-to-end ICSR lifecycle management and global safety operations.
The selected candidates will work on case processing, medical coding, narrative writing, quality review, and regulatory compliance activities while ensuring adherence to ICH, GVP, FDA, and EMA guidelines.
This is a full-time, permanent role based in Ahmedabad, offering exposure to international pharmacovigilance projects.
Vacancy Details (Official)
- Job Title: Pharmacovigilance Associate
- Company: Apcer Life Sciences
- Location: Ahmedabad, Gujarat
- Experience Required: 2–5 Years
- Employment Type: Full-time, Permanent
- Number of Openings: 5
- Industry: Pharmaceutical & Life Sciences
Roles & Responsibilities (Explained)
As a Pharmacovigilance Associate at Apcer Life Sciences, your day-to-day responsibilities will include:
- Handling end-to-end ICSR processing as per global safety regulations
- Booking, triaging, and data entry of safety cases into PV databases
- Performing MedDRA and WHO-DD coding accurately
- Writing clear, compliant medical narratives
- Preparing and sending follow-up queries to reporters
- Conducting literature review to identify valid adverse event cases
- Performing quality checks (QC) on processed cases
- Supporting aggregate reports like PSUR, PBRER, and DSUR (if applicable)
- Assisting in signal detection and ADR trend analysis
- Ensuring compliance with SOPs, client guidelines, and regulatory timelines
- Coordinating with global teams and project stakeholders
This role strengthens your foundation in global drug safety operations.
Eligibility Criteria (Official)
Educational Qualification
- UG: B.Pharm (Any Specialization)
- PG: M.Pharm (Any Specialization)
Experience Requirement
- Minimum 2 to 5 years of experience in Pharmacovigilance / Drug Safety
Skills Required (Explained)
To succeed in this role, candidates should have:
- Strong knowledge of pharmacovigilance and drug safety operations
- Practical experience in ICSR processing and safety data entry
- Hands-on expertise in MedDRA and WHO-DD coding
- Good command over medical narrative writing
- Understanding of global PV regulations (ICH, GVP, FDA, EMA)
- Strong attention to detail and quality mindset
- Excellent written and verbal communication skills
Salary Estimate
- Estimated Salary: ₹4,00,000 – ₹7,00,000 per annum
- Salary depends on experience, skill level, and project exposure
This is a competitive package for professionals with mid-level PV experience.
Interview Details
- Interview Mode: Not officially disclosed
- Likely to include technical PV interview + HR discussion
- Final details will be communicated by the Apcer Life Sciences HR team
Required Documents
Candidates should keep the following documents ready:
- Updated Resume / CV
- Educational certificates (B.Pharm / M.Pharm)
- Experience letters and relieving letters
- Government ID proof
- Passport-size photographs
How to Apply
Interested candidates can apply online through the official job portal:
Application Link:
https://www.naukri.com/job-listings-pharmacovigilance-associate-apcer-life-sciences-ahmedabad-2-to-5-years-070126013591
Apply as early as possible, as openings are limited.
FAQs – Pharmacovigilance Associate Job at Apcer Life Sciences
Q1. Is this job suitable for freshers?
No, this role requires 2–5 years of pharmacovigilance experience.
Q2. Is this a permanent job?
Yes, it is a full-time permanent position.
Q3. What PV activities are mainly involved?
ICSR processing, medical coding, narrative writing, QC, and regulatory compliance.
Q4. Can M.Pharm freshers apply?
Freshers are not eligible for this specific opening.
Q5. Where is the job location?
Ahmedabad, Gujarat.
Final Conclusion
The Pharmacovigilance Associate role at Apcer Life Sciences is an excellent opportunity for experienced PV professionals looking to work on global drug safety projects in a quality-driven organization. With strong exposure to international regulations, structured processes, and long-term career growth, this role can significantly enhance your pharmacovigilance career.
If you meet the eligibility criteria, do not miss this opportunity—apply today.
Note: Pharma Duniya does not charge any money for job information.
Candidates are advised to verify details from the official company website.
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