Navitas Life Sciences Job Openings: PV, Clinical Research & Investigator Roles | Apply Now

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