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Literature Review Specialist

Bengaluru, India
Start date
31 May 2024
Closing date
29 Jun 2024

View more

Medical Communications, Medical Writing
Full Time
Contract Type
Experience Level
Experienced (non-manager)

Job Details

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, Power Point, etc.).

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for 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.

Who will you be working for?

About ClinChoice

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. We are on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Join our passionate team and make a meaningful impact on global healthcare!

Our Company Ethos

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.

Key words: Literature Review, Literature Review Specialist, CRO, Contract Research Organisation



ClinChoice is a recognized and highly respected mid-size, global, full-service contract research organization (CRO) specializing in clinical development, post-marketing, and functional service support. We provide comprehensive end-to-end solutions, taking products from early clinical development to post-approval lifecycle management. We are committed to fostering innovation in the pharmaceutical, biotechnology, medical device & diagnostics, consumer health, cosmetics, and nutraceuticals industries. Since our establishment in 1995, we have consistently delivered high-quality services and solutions throughout the entire development lifecycle of our clients’ products. We serve a wide-ranging clientele that encompasses six of the top ten pharmaceutical companies, leading medical device companies, preeminent biotechnology companies, the largest consumer health and cosmetics companies, and numerous small-to-mid-sized innovator companies. With over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific, we are positioned to fulfil our clients’ needs locally and globally.


We’re on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.


Company info
+44 1628 566121
Suite G48
268 Bath Road

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