Pharma Jobs at Fortrea l PharmD/Mpharm/Bpharm Candidates Apply Now for Safety Science Coordinator II Role
Fortrea is hiring a Safety Science Coordinator II for its Pune location. If you hold a degree in Pharmacy, Nursing, Medical Sciences, or Life Sciences and have a passion for pharmacovigilance, this full-time opportunity allows you to be part of a global team dedicated to clinical safety excellence. Apply before July 29, 2025, to join a dynamic organization making a difference in global healthcare.
Welcome to Fortrea
Fortrea is currently seeking a Safety Science Coordinator II to join our team in Pune. If you have a passion for safety science and a background in Pharmacy, Nursing, Medical Sciences, Life Sciences, or a related area, we would love to hear from you.
Job Posting: Safety Science Coordinator II
Locations: Pune
Time Type: Full time
Time Left to Apply: End Date: July 29, 2025 (4 days left to apply)
Job Requisition ID: 253907
Job Overview
Assist with the overall Clinical Safety and/or PSS operations associated with products, including the adverse events process, which may include safety data collected from clinical trials and/or post-marketing setting (i.e., unsolicited reports). Manage and process expendable adverse events to the required standard
and submit them to the client and the regulatory agencies (if required) within the agreed/stated timelines.Responsible for providing this service to clients either as a support function to the client project groups or as a stand-alone business. Responsible for providing all clients, both internal and external, with the appropriate quality of service safely and cost-effectively. He/she will be expected to comply with the legal requirements of the Health and Safety at Work Act 1974, the COSHH regulations 1989, and the EC (European Commission) Directives 1992/3 as documented in the Company’s Health and Safety Manual.
Summary of Responsibilities
- Process adverse event reports from any source in accordance with the client/sponsor’s agreed-upon plans.
- Manage the receipt and processing of all adverse event reports reported either spontaneously from any source or in a clinical trial. This includes, but is not limited to:
– Data entry of safety data onto adverse event database(s) and tracking systems;
– Review of adverse events for completeness, accuracy, and appropriateness for expedited reporting.
– Write patient narratives and code adverse events accurately using MedDRA, if applicable.
– Determine lists against appropriate label (for Marketed products, if applicable).
– Identify clinically significant information missing from initial reports and generate queries for its collection, consulting the medical staff if needed.
Qualifications (Minimum Required)
- PharmD/Mpharm/Bpharm + 2 years of relevant experience.
- Degree preferred to be in one or more of the following disciplines: Pharmacy, Nursing, Medical Sciences, Life Sciences, or related area.
Experience (Minimum Required)
- High degree of accuracy with attention to detail.
- Functions as a team player and offers peer support as needed.
- Good written and verbal communication skills.
- Ability to work independently with moderate supervision.
- Preferred Qualifications Include
– Office Environment
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