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Safety Specialist Ii

Navitas Life Sciences
Navitas Life Sciences
0-3 years
Not Disclosed
10 Jan. 5, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Opening: Safety Specialist II – Pharmacovigilance / Drug Safety
Location: Bangalore, India
Employment Type: Full-Time
Category: Pharmacovigilance / Regulatory Affairs

About the Role
We are seeking a Safety Specialist II to join our growing pharmacovigilance team. In this role, you will contribute to aggregate safety reporting, signal detection, and risk management activities while ensuring compliance with global regulatory requirements. The position is ideal for life sciences professionals looking to grow in drug safety and regulatory affairs within a global healthcare environment.

Key Responsibilities

Aggregate Reports:

  • Author, review, and finalize Aggregate Safety Reports including DSURs, PBRERs, PSURs, PADERs, and other client-specific reports.

  • Extract and analyze safety data from databases, generate line listings (LL) and summary tabulations (ST), and incorporate into reports.

  • Perform literature screening for significant safety articles and include them in relevant report sections.

  • Compile benefit-risk evaluation sections provided by medical reviewers.

  • Ensure adherence to internal and external timelines; address comments from internal or client reviewers.

  • Participate in audits and inspections by clients and health authorities.

Signal Management & Risk Management Plans:

  • Screen and analyze safety data to identify potential signals, including frequency tabulations and signal estimation using approved tools.

  • Draft signal detection, validation, assessment, and prioritization reports based on available data.

  • Track and monitor the status of signals (potential, open, refuted, validated).

  • Support the development of Risk Management Plans and associated pharmacovigilance activities as per SOPs.

Desirable Skills & Qualifications:

  • Graduate or post-graduate degree in Life Sciences, Pharmacy, Medicine, Dentistry, or Allied Health Sciences.

  • Proven ability to author and review aggregate safety reports, particularly PBRERs.

  • Knowledge of GCP, GVP, ICH, USFDA, and other global pharmacovigilance guidelines.

  • Basic medical and therapeutic terminology competence.

  • Strong understanding of patient safety and regulatory obligations.

  • Familiarity with pharmacovigilance databases (e.g., Argus) and regulatory reporting processes.

  • Proficient in MS Office (Word, Excel, PowerPoint).

  • Excellent written and verbal communication skills in English; additional languages are a plus.

  • Strong analytical, organizational, and teamwork skills, with attention to detail and reliability.

Experience: Entry-level to 3 years preferred for candidates with relevant pharmacovigilance, regulatory affairs, or medical writing exposure.

Why Join Us:

  • Work in a dynamic global pharmacovigilance environment.

  • Exposure to aggregate reporting, signal detection, and risk management activities.

  • Opportunities for professional growth in drug safety, regulatory affairs, and clinical research.

Apply Now to join a leading healthcare organization and advance your career in pharmacovigilance and drug safety.