Medical Librarian
- Location
- Pune
- Work mode
- On-site
- Employment type
- Full-time
About the job
Role Overview We are seeking a detail-oriented and research-savvy librarian to support our pharmacovigilance team by conducting systematic literature searches to identify safety signals, adverse drug reactions (ADRs), and emerging safety information. This role is critical for ensuring compliance with global regulatory requirements and maintaining the safety profile of our products. Key Responsibilities
• Design and execute comprehensive literature search strategies using databases such as PubMed, Embase, Scopus, and Web of Science.
- Design and execute comprehensive literature search strategies using databases such as PubMed, Embase, Scopus, and Web of Science.
- Monitor and retrieve relevant publications for Individual Case Safety Reports (ICSRs), Periodic Safety Update Reports (PSURs), and Development Safety Update Reports (DSURs).
- Maintain documentation of search strategies, results, and rationale to support regulatory audits and inspections.
- Collaborate with pharmacovigilance scientists, medical writers, and regulatory affairs teams to ensure timely and accurate reporting.
- Stay current with Good Pharmacovigilance Practices (GVP), especially Module VI, and other global safety regulations.
• Master’s degree in Library Science, Information Management, or a related field.
- Master’s degree in Library Science, Information Management, or a related field.
- Minimum 2 years of experience in biomedical literature searching, preferably in a pharmaceutical or healthcare setting.
- Familiarity with medical indexing systems (e.g., MeSH, Emtree) and Boolean logic.
- Understanding of pharmacovigilance principles and regulatory frameworks (e.g., EMA, FDA, ICH).
- Strong attention to detail and ability to manage multiple priorities under tight deadlines.
- Experience with reference management tools (e.g., EndNote, Mendeley).
- Knowledge of drug safety databases and signal detection methodologies.
- Certification in pharmacovigilance or drug safety (e.g., DIA, PV training programs) is a plus.
- Analytical thinking: Strong analytical skills to evaluate complex medical information and identify relevant safety data.
- Communication: Excellent written and verbal communication skills to interact with internal teams, regulators, and medical professionals.
Learn more about our EEO & Accommodations request here .
From FTMEX Fortrea Clinical Development Mexico S.DeR.L.DeC.V.'s careers page (Workday), checked 30 Oct 2026.
How to apply
- Select Apply on fortrea.wd1.myworkdayjobs.com. It opens FTMEX Fortrea Clinical Development Mexico S.DeR.L.DeC.V.'s own application form in a new tab, run on Workday.
- Fill in the form and upload your résumé there. Jobiwork never sees your application.
- FTMEX Fortrea Clinical Development Mexico S.DeR.L.DeC.V. will reply to you directly. No real employer asks you for money to apply.
Posted 6 Oct 2026 · checked 30 Oct 2026 · Report this job