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Specialist Drug Safety

3+ years
₹10–15 LPA
9 July 26, 2025
Job Description
Job Type: Full Time Education: MSc/MPH/MPharm 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

Specialist – Drug Safety
Location: Mumbai, Maharashtra, India
Work Mode: Hybrid
Work Type: Full-time
Estimated Salary: ₹10–15 LPA (based on experience and market standards)


About the Role:
As a Specialist – Drug Safety at ADVANZ PHARMA, you will be part of the Medical Office team, contributing expert knowledge in drug safety and medical affairs. You will play a key role in pharmacovigilance activities, medical writing, compliance tracking, signal detection, and regulatory documentation. This role requires collaborative interaction across global teams and functions, ensuring all safety-related tasks are performed efficiently and in compliance with global regulations.


Key Responsibilities:

  • Draft and review Periodic Safety Update Reports (PSURs) and Periodic Adverse Drug Experience Reports (PADERs) from a medical perspective.

  • Prepare and manage signal reports including DSR, DEP, SAR, and ensure quality and compliance in signal detection.

  • Support preparation of ad hoc safety reports such as RMPs, Clinical Evaluation Summaries (CES), and regulatory health authority responses.

  • Conduct medical writing to support clinical evaluations and product safety reviews.

  • Oversee safety-related variations and ensure up-to-date product information.

  • Ensure compliance with Good Pharmacovigilance Practices (GVP) and participate in audits and inspections.

  • Track compliance using systems like PSMF and safety databases.

  • Stay updated on global PV regulations, especially across Europe and RoW.

  • Represent ADVANZ PHARMA during scientific meetings, audits, and inspections.

  • Interact with regulators, healthcare professionals, and patients from a safety standpoint when required.

  • Demonstrate leadership in promoting company values: Entrepreneurship, Speed, and Integrity.

  • Collaborate across departments and contribute to making ADVANZ PHARMA a desirable workplace.


Candidate Profile:

Qualifications:

  • Bachelor’s degree in Life Sciences or Pharmacy.

  • Postgraduate qualification (e.g., MSc, MPH, MPharm) in a relevant field preferred.

Experience and Skills:

  • Strong experience in Pharmacovigilance or Drug Safety within the pharmaceutical industry.

  • Solid background in medical writing, especially for PSURs, RMPs, and regulatory dossiers.

  • Proficiency in compliance tracking and handling PV audits.

  • Strong analytical and problem-solving skills.

  • Excellent communication and interpersonal skills, with the ability to work across time zones and cultures.

  • A growth-oriented mindset, adaptability, and a proactive approach to challenges.

  • Ability to function effectively in a fast-paced, entrepreneurial, and collaborative environment.


Why Join ADVANZ PHARMA?

  • Work in a diverse, global environment focused on improving patient outcomes.

  • Contribute to a mission-driven company with clear values of integrity and innovation.

  • Be part of a dynamic culture that fosters career growth, collaboration, and continuous learning.

  • Make a meaningful impact in a company that encourages entrepreneurship and values your ideas.