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Safety Specialist – Pharmacovigilance

Thermo Fisher Scientific
Thermo Fisher Scientific
4+ years
₹8–12 LPA
10 July 26, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Safety Specialist – Pharmacovigilance (Remote)
Location: Remote (India-based candidates preferred)
Work Type: Full-time
Estimated Salary: ₹8–12 LPA (based on 4+ years of experience and remote flexibility)


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About the Organization:
Join a leading global organization driving innovation in pharmacovigilance and clinical research. With a strong reputation in drug safety monitoring and compliance with global regulations, this company offers a growth-centric and collaborative environment for professionals in life sciences.


Job Title: Safety Specialist – Pharmacovigilance
Experience Required: Minimum 4 years
Work Mode: Fully Remote


Key Responsibilities:

  • Perform end-to-end PV case processing: data entry, coding, medical review, and narrative writing.

  • Assess and evaluate Adverse Events (AEs) for completeness, accuracy, and compliance.

  • Prepare and submit regulatory safety reports including SUSARs and PSURs.

  • Collaborate with internal teams, investigators, clients, and third-party vendors.

  • Participate in audits, kick-off meetings, and investigator meetings.

  • Stay current with evolving global PV regulations and guidelines.

  • Mentor and guide junior PV staff, supporting training and process improvements.


Candidate Requirements:

Education:

  • Bachelor's degree in Pharmacy, Life Sciences, or a related discipline.

Experience:

  • Minimum 4+ years in pharmacovigilance, with hands-on experience in clinical trial and post-marketing case processing.

Technical Skills:

  • Proficiency in Argus Safety Database.

  • Strong skills in Microsoft Office (Excel, Word, Outlook).

Regulatory Knowledge:

  • Sound understanding of ICH-GCP, FDA, EMA, and global PV regulations.

Soft Skills:

  • Detail-oriented with strong communication, analytical, and problem-solving abilities.


Why Apply?

  • 100% Remote – Flexible working from anywhere in India

  • Work with industry-leading safety databases and practices

  • Competitive salary and benefits

  • Career growth opportunities in a global PV organization


To Apply:
Interested candidates should apply through PharmaBharat's trusted platform or reach out through the official career portal or recruiter contact provided by the employer.