Life Science Jobs at Fortrea 2025 | Apply Now
Fortrea, a trusted global leader in clinical research and life sciences solutions, is hiring a Safety Science Coordinator II in Bangalore. This full-time role offers professionals with experience in drug safety and pharmacovigilance the opportunity to contribute to global clinical safety operations, manage adverse event reporting, and ensure compliance with international regulatory standards. If you have a strong background in life sciences and a passion for patient safety, this role could be your next career move.
- Job Position: Safety Science Coordinator II
- Location: Bangalore, India
- Job ID: 254692
- Last Date: September 28, 2025
About the Company:
Fortrea is a global contract research organization (CRO) providing clinical trial management, safety, pharmacovigilance, and regulatory services to pharmaceutical, biotechnology, and life sciences companies. With a strong focus on innovation, compliance, and quality, Fortrea empowers its clients to bring safe and effective treatments to market.
Education:
Degree in Life Sciences
Experience:
- 2-3 years of drug safety experience
- Experience in clinical trial case processing
- High accuracy, attention to detail, teamwork, and communication skills
- Proficiency in MS Office, Windows applications, and mentoring skills preferred
Job Description:
As a Safety Science Coordinator II, you will assist in the
operation of Clinical Safety and PSS, focusing on products, including managing adverse event data from clinical trials and post-marketing reports. Your responsibilities will include processing adverse events, ensuring timely submission to clients and regulatory agencies, and delivering high-quality service safely and cost-effectively.Key Responsibilities:
- Process adverse event reports according to client/sponsor plans
- Manage receipt and processing of adverse event reports, including data entry and review
- Write patient narratives, code adverse events, and ensure appropriate medical review
- Submit expedited reports to relevant stakeholders within specified timelines
- Assist in quality review, database reconciliation, and documentation maintenance
- Support training of staff, generate metrics, and ensure compliance with regulations
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