Remote Pharmacovigilance Job at IQVIA
A rare chance has emerged for medical professionals to join IQVIA as a Sr Medical Safety Advisor in Bengaluru. This is a full-time, home-based position. The Remote Pharmacovigilance Job invites qualified candidates to apply their expertise in pharmacovigilance and safety data evaluation. Applications are open now.
About IQVIA:
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The organisation is dedicated to creating intelligent connections that accelerate the development and commercialisation of innovative medical treatments, ultimately improving patient outcomes and population health worldwide. With a strong commitment to integrity, IQVIA ensures a transparent hiring process and maintains high standards of professionalism.
Job Details:
- Job Title: Sr Medical Safety Advisor
- Location: Bengaluru, India
- Job Type: Full-time, Home-based
- Reference Number: R1569515
Job Description:
The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process. The role involves determining the medical and scientific relevance of serious adverse event reports within the context of the product’s safety profile and participating in matrix management activities, including preparation and evaluation of safety issues.
Key Responsibilities:
- Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs).
- Compose, edit, and medically review Analyses of Similar Events (AOSE) for expedited cases.
- Provide coding review of AEs, SAEs, and other medical data listings.
- Serve as an internal consultant to pharmacovigilance case processing teams.
- Perform medical safety review of protocols and case report forms for appropriate safety content in the Remote Pharmacovigilance Job.
- Provide aggregate reviews of safety information to maintain oversight of a product’s safety profile.
- Ensure service delivery from productivity, compliance, and quality perspectives.
- Lead training activities and participate in audit preparation and knowledge exchange initiatives.
Eligibility Criteria for the Remote Pharmacovigilance Job:
- A medical degree from an accredited and internationally recognised medical school.
- Three years of experience practising clinical medicine after the award of the medical degree.
- Two years of pharmaceutical experience is preferred.
- Sound knowledge of Medicine and in-depth knowledge of clinical research regulatory requirements.
- Good communication skills, both verbal and written.
- A valid medical license, or equivalent, from the country or region of residence is preferred.
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