Fortrea Hiring Pharma Graduates for Safety Science Specialist Role – Apply Now
Looking for a Pharmacovigilance Job in Bangalore? Fortrea is hiring a Safety Science Specialist to support clinical and post-marketing safety operations. This opportunity is especially relevant for candidates searching for Pharm D Jobs, with responsibilities covering AE/SAE case processing, safety narratives, MedDRA coding, expedited reporting, periodic safety reports, and regulatory submissions.
- Job Position: Safety Science Specialist
- Location: Bangalore
- Job Requisition ID: 261470
About The Company
Fortrea is a leading organization in the pharmaceutical sector, dedicated to ensuring the safety and efficacy of medical products. With a strong focus on pharmacovigilance, Fortrea operates globally, providing critical services that support the development and monitoring of pharmaceuticals. The company is committed to maintaining high standards of safety and compliance, making it an ideal workplace for professionals seeking to advance their careers in pharmacovigilance.
Job Description
The Safety Science Specialist will support pharmacovigilance operations by processing adverse event reports from clinical trials and post-marketing sources. This Pharmacovigilance Job involves safety database entry, case assessment, narrative writing, MedDRA coding, follow-up activities, expedited reporting, periodic safety reporting, quality review, and regulatory compliance.
Key Responsibilities
- Manage the receipt and processing of all adverse event reports, including data entry into safety databases.
- Review adverse events for completeness and accuracy, ensuring appropriate expedited reporting.
- Write patient narratives and code adverse events accurately using MedDRA.
- Identify missing clinically significant information and ensure its collection.
- Ensure all cases requiring expedited reporting are processed within required timelines.
- Assist with database reconciliation in collaboration with the Data Management team.
- Support preparation for client meetings and liaise with clients as necessary.
- Participate in audits and inspections, preparing documentation as needed.
Eligibility Criteria
- Non-degree + 2 years of safety experience or 3-4 years of relevant experience.
- Associate degree + 2 years of safety experience or 2-3 years of relevant experience.
- BS/BA + 1 year of safety experience or 2 years of relevant experience.
- MS/MA + 1 year of safety experience or 1-2 years of relevant experience.
- PharmD + 1 year of safety experience or 1-2 years of relevant experience.
- Relevant experience in the pharmaceutical, biotechnology, or CRO industry is preferred.
Required Skills
- High degree of accuracy and attention to detail.
- Strong written and verbal communication skills.
- Ability to work independently with minimal supervision.
- Proficiency in MS Office and Windows applications.
- Training and mentoring skills are preferred.
Why Join Fortrea?
Joining Fortrea offers a unique opportunity to be part of a dedicated team focused on pharmacovigilance and safety science. The organization values accuracy, compliance, and quality service, providing an environment where professionals can thrive and develop their skills. With a commitment to safety and regulatory standards, Fortrea is an excellent choice for those looking to advance their careers in the pharmaceutical industry.
For candidates exploring Pharm D Jobs, this Pharmacovigilance Job offers hands-on exposure to adverse event processing, patient safety narratives, MedDRA coding, expedited reporting, regulatory submissions, and global safety operations. It is particularly relevant for professionals seeking to develop their careers in Drug Safety and Pharmacovigilance.
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