Pharmacovigilance Specialist (Case Processing)

Status
Open
Remote policy
Remote
Employment type
Not stated
Salary
Not stated
Categories
PV-RA-MI-Operations, Pharmacovigilance, Case-Processing, Clinical-safety, Regulatory-Affairs, Pharmacovigilance-Specialist, Pharmacovigilance-Analyst, Pharmacovigilance-Associate, Pharmacovigilance-Coordinator, Pharmacovigilance-Officer
Source
himalayas
First observed
2026-08-21 13:14 UTC
Last seen
2026-08-21 13:14 UTC
Source claims posted
2026-08-21 12:38 UTC
Consecutive misses
1 of 10

What the posting says

The Pharmacovigilance Specialist will be responsible for ensuring the operational delivery of assigned tasks at the project level, with a focus on safety case reporting, processing of safety case report data, and literature screening activities. The role involves communication with the Pharmacovigilance Team Leader and Pharmacovigilance Manager regarding potential risks related to operational delivery, quality standards, client relationships, and the company's reputation, as well as addressing ad hoc project tasks and requirements.

CV must be in English language for further assessment.

Position is full-time remote/home-based in any European country and Turkey.

Responsibilities:

Oversee and manage the workflow of safety case reports, ensuring efficient processing

Perform triage on safety case reports to assess priority and necessary actions

Review, manage, and file source documentation in compliance with regulatory requirements

Process safety case reports, including SDB data entry, narrative writing, seriousness assessment, medical review (including causality and expectedness assessments), and reporting requirements evaluation

Conduct follow-up activities and manage queries related to safety case reports

Execute quality control checks on data entry and case processing to ensure accuracy and compliance

Reconcile safety case reports to ensure consistency and completeness of data

Prepare line listings to summarize and report on safety case data

Requirements

University degree in Life Science field

At least 1 year of experience in Safety and Pharmacovigilance within the pharmaceutical or Contract Research Organization (CRO) industry

Experience of clinical trial case processing in a safety database.

Proficiency in both verbal and written local language and English

Strong expertise with MS Office

Beneficial experience with Veeva Vault Safety system

Knowledge of EU GVP modules and applicable global safety regulations (e.g. ICH, FDA reporting requirements)

Benefits

Full remote flexible work

Professional growth and career opportunities

International team and environment

Originally posted on Himalayas

Quality

Completeness: 65%

Not enough history yet to judge honesty signals.

Timeline

  1. *
    #241932 2026-08-21 13:14 UTC
    Published
  2. o
    #243894 2026-08-21 13:39 UTC
    Not seen
    Miss 1 in a row