Navitas Life Sciences is a global clinical research organization (CRO) headquartered in Princeton, NJ, with 1,000+ employees across 5 countries. The company specializes in drug development, regulatory & safety services, and clinical data sciences, helping biopharmaceutical firms accelerate life-saving therapies.
As an HIG Portfolio company, Navitas offers end-to-end CRO services, including pharmacovigilance (PV), clinical trial management, and regulatory compliance solutions. Their expertise ensures cost efficiency, regulatory adherence, and innovation in clinical research.
Current Job Openings
1. DSA/SDSA-ICSR (Pharmacovigilance) – Bengaluru
Key Responsibilities:
- Perform data entry of Individual Case Safety Reports (ICSR) into safety databases.
- Ensure compliance with global regulatory guidelines (MedDRA, WHO-DD).
- Code medical history, events, and drugs using standardized dictionaries.
- Prepare safety narratives and conduct quality checks before submission.
- Generate follow-up queries and address case corrections.
- Collaborate with medical reviewers & quality teams.
Eligibility:
- Education: MPharm / BPharm
- Experience: 1-5 years in PV & end-to-end case processing
- Skills: Pharmacovigilance, MedDRA coding, regulatory compliance
2. Clinical Research Associate (BA/BE) – Udupi/Manipal
Key Responsibilities:
- Act as Sub-Investigator in clinical studies.
- Review protocols, ICFs, and clinical study reports (CSR).
- Monitor subject dosing, adverse events (AEs), and study compliance.
- Ensure adherence to ICH-GCP, CDSCO, USFDA, and WHO guidelines.
- Prepare clinical raw data, confinement reports, and summaries.
- Coordinate with QA, sponsors, and regulatory teams.
Eligibility:
- Education: BPharm / MPharm
- Experience: 1-5 years in clinical research
- Skills: ICH-GCP, regulatory guidelines, clinical trial execution
3. Clinical Investigator – Manipal
Key Responsibilities:
- Screen & assess volunteer eligibility for clinical trials.
- Monitor and report adverse events (AEs/SAEs).
- Maintain emergency drugs, ICU setup, and GCP-compliant records.
- Coordinate with Principal Investigators (PIs) and study teams.
Eligibility:
- Education: MBBS (Medical Council registration required)
- Experience: 0-2 years in clinical research
- Skills: Patient screening, AE monitoring, GCP compliance
Why Join Navitas Life Sciences?
✅ Global exposure in pharma & clinical research
✅ Cutting-edge technology in drug development
✅ Career growth in PV, regulatory affairs, and CRO services
✅ Competitive salary & benefits
How to Apply?
For Bangalore Send Resume On This : recruitment.bangalore@navitaslifesciences.com
For Manipal/ Udupi Send Resume On This : recruitment.india@navitaslifesciences.com
