Clinical Research Jobs at Fortrea
Looking for Clinical Research Jobs in India’s fast-growing pharmaceutical and CRO industry? Fortrea Jobs has announced an exciting opportunity for the position of Safety Science Coordinator-II in Bangalore. This is an excellent opportunity for graduates and postgraduates in Life Sciences, Pharmacy, Nursing, Biological Sciences, and Medical Sciences who want to build a rewarding pharmacovigilance and clinical safety career. If you’re searching for Life Science Jobs with a globally recognized clinical research organization, don’t miss this opportunity to join Fortrea and contribute to global drug safety programs.
About Fortrea
Fortrea is a leading global Contract Research Organization (CRO) providing clinical development, patient access, and technology solutions to pharmaceutical, biotechnology, and medical device companies worldwide. The company specializes in clinical operations, pharmacovigilance, regulatory support, and drug development services, helping bring innovative therapies safely to patients across the globe. Fortrea is recognized for its commitment to quality, compliance, scientific excellence, and employee development, making it one of the preferred employers for professionals seeking Life Science Jobs.
Job Details
- Position: Safety Science Coordinator II
- Location: Bangalore
- Employment Type: Full-Time
- Application Deadline: 14th July 2026
Key Responsibilities
- Process adverse event reports from clinical trials and post-marketing sources as per client requirements.
- Perform data entry of safety information into adverse event databases and tracking systems.
- Review adverse event reports for completeness, accuracy, and expedited reporting requirements.
- Prepare patient narratives and accurately code adverse events using MedDRA, where applicable.
- Identify missing clinical information and raise queries for follow-up.
- Ensure cases undergo appropriate medical review.
- Prioritize and process cases requiring expedited reporting within regulatory timelines.
- Submit Serious Adverse Event (SAE) reports to clients, regulatory authorities, ethics committees, investigators, partners, and project teams within study timelines.
- Support preparation and submission of Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs).
- Maintain project documentation, tracking systems, and study files.
- Perform database reconciliation and related safety activities.
- Conduct quality or peer review of processed safety reports.
- Support training and mentoring of team members.
- Assist in generating project metrics and monthly status reports.
- Follow SOPs, work instructions, and regulatory guidelines related to pharmacovigilance and safety reporting.
- Participate in client meetings and support client communications when required.
- Assist in quality issue management, audits, and inspection readiness.
- Ensure compliance with study protocols, regulatory requirements, and quality standards.
- Perform additional responsibilities assigned by management.
Qualifications
Applicants should have one of the following:
- Non-degree qualification with 1 year of Safety experience or 3 years of relevant experience, or
- Associate Degree with 1 year of Safety experience or 2 years of relevant experience, or
- Bachelor’s degree (BS/BA) with 1 year of relevant experience, or
- Master’s degree (MS/MA) with 1 year of relevant experience, or
- PharmD with 1 year of relevant experience (one-year residency/fellowship may be considered).
Preferred Educational Background
- Biological Sciences
- Life Sciences
- Related disciplines
Required Skills
- High attention to detail and accuracy.
- Good written and verbal communication skills.
- Ability to work independently with moderate supervision.
- Strong teamwork and collaboration skills.
- Good keyboard proficiency.
- Working knowledge of Microsoft Office and Windows applications.
- Mentoring skills are preferred.
