Navitas Life Sciences has announced exciting career opportunities for Drug Safety Associates in Bangalore and Chennai. If you have 1โ3 years of core clinical trial case processing experience, this is an excellent opportunity to advance your career in Pharmacovigilance with a leading global life sciences organization.
The company is looking for immediate joiners with hands-on experience in clinical trial case processing. Candidates without clinical trial case processing experience and freshers are not eligible for this role.
If you’re searching for Drug Safety Associate jobs in Bangalore, Pharmacovigilance jobs in Chennai, or clinical trial case processing jobs in India, this opportunity is worth exploring.
Job Details
| Details | Information |
|---|---|
| Position | Drug Safety Associate |
| Company | Navitas Life Sciences |
| Location | Bangalore, Chennai |
| Experience | 1โ3 Years |
| Employment Type | Full-Time |
| Department | Pharmacovigilance |
| Preferred Candidates | Immediate Joiners |
Key Responsibilities
As a Drug Safety Associate, you may be responsible for:
- Processing clinical trial adverse event cases accurately.
- Reviewing and evaluating safety data received from clinical studies.
- Ensuring compliance with global pharmacovigilance regulations.
- Maintaining quality standards and meeting turnaround timelines.
- Performing data entry and medical coding where applicable.
- Supporting case reconciliation and follow-up activities.
- Collaborating with global safety teams and stakeholders.
- Following SOPs, ICH-GCP guidelines, and regulatory requirements.
Eligibility Criteria
Candidates should have:
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Nursing, Medicine, Biotechnology, or related healthcare discipline.
- 1โ3 years of core Clinical Trial Case Processing experience.
- Good understanding of Pharmacovigilance principles.
- Experience handling clinical trial safety cases.
- Strong communication and analytical skills.
- Ability to work in a fast-paced global environment.
Important:
- Freshers are not eligible.
- Candidates without Clinical Trial Case Processing experience should not apply.
Preferred Skills
- Clinical Trial Safety Case Processing
- Pharmacovigilance
- Adverse Event Management
- ICSR Processing
- MedDRA Coding
- Safety Database Exposure (Argus preferred)
- Quality Compliance
- Regulatory Guidelines (ICH-GCP)
Why Join Navitas Life Sciences?
- Opportunity to work with global pharmaceutical clients.
- Exposure to international clinical trial projects.
- Career growth in Pharmacovigilance.
- Collaborative work culture.
- Learning and development opportunities.
- Competitive salary and employee benefits.
Salary (Estimated)
Based on current market trends, the expected salary for this role is approximately:
โน4.5 LPA โ โน8.5 LPA (CTC)
Actual compensation depends on experience, interview performance, and company policies.
How to Apply
Interested and eligible candidates can share their updated CV at:
Email: recruitment.bangalore@navitaslifesciences.com
Subject Line: Application for Drug Safety Associate โ Bangalore/Chennai
Apply as early as possible since immediate joiners are preferred.