Explore Exciting Pharmacovigilance Jobs at Fortrea Careers in Pune| Apply Now
Looking to build your career in pharmacovigilance and clinical safety? Explore exciting opportunities with Fortrea Careers through the Safety Science Coordinator I role in Pune. This full-time position is perfect for graduates or professionals aiming to advance in pharmacovigilance jobs and pharma jobs in Pune. You’ll contribute to ensuring drug safety, managing adverse event reports, and maintaining compliance with global regulatory standards—helping Fortrea deliver safer therapies worldwide.
- Job Position :Safety Science Coordinator I
- Location: Pune, India
- Job Requisition ID: 255152
- Employment Type: Full-time
- Application Deadline: October 31, 2025
About the Company
Fortrea is a global leader in clinical development and technology-enabled services for the pharmaceutical and biotechnology industries. As part of Fortrea Careers, you’ll be joining a company committed to innovation, compliance, and patient safety. Fortrea partners with life science organizations worldwide to accelerate the delivery of life-changing medicines, offering rewarding pharmacovigilance jobs and opportunities across global pharma hubs like Pune.
Job Description: Fortrea Careers in Pharmacovigilance Jobs
As a Safety Science Coordinator I, you will play a vital role in pharmacovigilance operations and clinical safety management. Your primary responsibility includes processing and reporting adverse event data, managing safety reports, and ensuring compliance with regulatory authorities. This is an excellent opportunity for professionals looking to enhance their expertise through Fortrea Careers in pharma jobs in Pune, especially those targeting pharmacovigilance jobs.
Key Responsibilities in Pharmacovigilance Jobs
- Process Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs).
- Maintain adverse event tracking systems and safety project documentation.
- Prepare and submit ESRs and PSRs to clients and regulatory bodies, in line with expectations of pharmacovigilance jobs.
- Perform patient narrative writing and MedDRA coding for adverse events.
- Conduct listedness assessments for marketed products.
- Generate queries and reconcile safety data.
- Support peer review of reports and ensure regulatory compliance.
- Mentor PSS assistants and coordinate safety meetings.
Qualifications
- Bachelor’s or Master’s in Life Sciences, Pharmacy, Nursing, or Medical Sciences.
- 0–2 years of experience in pharmacovigilance, clinical safety, or related areas, targeting pharmacovigilance jobs.
- Excellent English communication skills (verbal and written).
- Proficiency in MS Office and familiarity with safety databases preferred.
- Strong attention to detail and logical accuracy.
Preferred Experience
-
Prior exposure to adverse event processing and regulatory submissions.
-
Work experience in pharmaceutical, biotechnology, or CRO organizations.
-
Ability to collaborate effectively and manage multiple safety-related tasks
Work Environment :Pharma Jobs in Pune
This position offers a professional office or remote work setup, promoting flexibility and a supportive environment. Fortrea Careers encourage growth through continuous learning and collaboration in a globally recognized pharmacovigilance framework. Positions like these are an excellent entry into pharmacovigilance jobs.
