ClinChoice Literature Review Specialist Position! Pharma Candidates Apply
Literature Review Specialist
at ClinChoice (View all jobs)
Bangalore or Hyderabad – India
ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our in-house team as a Literature Review Specialist on a permanent basis. You will work on projects from our varied client base, ranging from small to big pharmaceutical, biotechnology, medical device, and consumer health companies.
Join our team: you can be part of making a difference in peoples’ lives and experience a fulfilling and rewarding career!
Main Job Tasks and Responsibilities:
- Reviews literature for Client Consumer or Pharma products for safety information as detailed in applicable Client procedures and assess for potential ICSRs, signals, and/or meeting PBRER-PSUR criteria and as required.
- Responsible for translation management and full text procurement, as detailed in applicable client procedures.
- Authors narratives/summaries/MAH comments as per client SOPs.
- Provides medical/safety support on all assigned Client Consumer or Pharma products.
- Escalates any identified ICSRs, PSUR relevance, and potential signals to the Literature Review Physician and/or client within agreed timelines mandated by client procedures.
- Completes the assessment of literature references for aggregate reports within prescribed timelines.
- Accurately completes required documentation and verifiable data, then uploads to Client designated repository.
- Completes monthly tracker with details of assessments made within the client system/tools.
- Provides monthly metrics with accurate and verifiable data.
- Awareness and understanding of relevant GVP modules.
Education and Experience:
- MSc, BPharm, PharmD, MPharm with 2 years of Pharmacovigilance experience, including global literature monitoring.
- Experience in literature research and interpretation of safety data.
- Knowledge of international regulatory requirements and guidance (International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) and GVP).
- Training and mentoring skill (GVP concepts & its application).
- Must have basic hands-on experience with MS office applications (Outlook, Excel, Word, PowerPoint, etc.).
The Application Process
Once you have submitted your CV, you will receive an acknowledgment that we received it. If you have the requirements we need, you will be invited for a phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Apply for this position here
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