Apply for Safety Science Coordinator job in Pune at Fortrea. Freshers and experienced candidates in pharmacovigilance can apply online now.
Are you looking to build a career in pharmacovigilance and clinical safety within a reputed global CRO? This is an excellent opportunity for life sciences and pharmacy graduates to enter or grow in the drug safety domain. A leading clinical research organization is inviting applications for the role of Safety Science Coordinator I in Pune, offering hands-on exposure to adverse event processing and regulatory compliance.
Company Overview
Fortrea is a globally recognized contract research organization (CRO) that delivers comprehensive clinical development and patient access solutions. With a strong presence in clinical trials, pharmacovigilance, and regulatory services, the company supports pharmaceutical, biotechnology, and medical device organizations worldwide. Known for its quality-driven approach, Fortrea provides a collaborative work environment focused on innovation and compliance.
Job Overview
| Job Title | Safety Science Coordinator I |
|---|---|
| Company | Fortrea |
| Location | Pune, India |
| Employment Type | Full-Time |
| Department | Clinical Safety / Pharmacovigilance |
| Experience | 0–2 Years |
| Qualification | Life Sciences / Pharmacy / Medical Background |
| Application Deadline | March 24, 2026 |
Job Location & Employment Type
- Work Location: Pune, Maharashtra
- Job Type: Full-time
- Work Environment: Office-based or remote (as per company policy)
Open Positions / Department Details
This role is part of the Clinical Safety and Pharmacovigilance (PSS) team. The selected candidate will contribute to drug safety operations involving adverse event management, regulatory submissions, and safety database maintenance.
Key Roles & Responsibilities
As a Safety Science Coordinator I, you will be actively involved in end-to-end pharmacovigilance activities. Your responsibilities will include:
- Supporting the processing and submission of Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs)
- Maintaining and updating adverse event tracking systems
- Assisting in the documentation and organization of project and safety files
- Recording and managing Adverse Event (AE) and Serious Adverse Event (SAE) data
- Performing data entry into pharmacovigilance databases with high accuracy
- Preparing patient safety narratives based on case data
- Coding adverse events using standardized medical terminology such as MedDRA
- Conducting listedness assessments for marketed products when applicable
- Generating and managing queries to resolve incomplete or inconsistent safety data
- Ensuring timely submission of safety reports to:
- Regulatory authorities
- Ethics committees
- Investigators and clients
- Participating in quality checks and peer reviews of processed safety cases
- Assisting in database reconciliation activities
- Maintaining global safety reporting requirements across different regions
- Adhering to Standard Operating Procedures (SOPs) and internal quality systems
- Supporting archival processes for completed clinical studies
- Coordinating internal and external meetings or communications
- Providing guidance and support to junior team members when required
- Ensuring compliance with all applicable regulatory and safety standards
- Performing additional administrative or operational tasks as assigned
Eligibility Criteria
Educational Qualification
Candidates from the following backgrounds are eligible:
- B.Pharm / M.Pharm / Pharm.D
- B.Sc / M.Sc (Life Sciences, Biological Sciences, Medical Sciences)
- Nursing or related healthcare qualifications
- Equivalent degrees in relevant disciplines
Experience Required
- Freshers or candidates with 0 to 2 years of experience in:
- Pharmacovigilance
- Clinical safety
- Regulatory affairs
- Clinical data management
- Medical affairs
- Candidates with internship, residency, or fellowship experience (especially Pharm.D) will also be considered.
Skills Required
- Strong attention to detail and data accuracy
- Good written and verbal communication skills in English
- Ability to manage multiple tasks and meet deadlines
- Basic knowledge of pharmacovigilance processes
- Familiarity with MS Office tools (Word, Excel, Outlook)
- Understanding of safety databases and regulatory requirements (preferred)
- Analytical thinking and problem-solving ability
- Team collaboration and coordination skills
Salary & Benefits
- Salary will be as per company norms
- Additional benefits may include:
- Health insurance
- Career development programs
- Exposure to global clinical projects
- Learning and training opportunities
Selection Process
The hiring process may include:
- Application screening
- HR interview
- Technical/functional interview
- Final selection and offer
How to Apply
Interested and eligible candidates should apply through the official online application portal before the deadline.
- Ensure your resume is updated with relevant pharmacovigilance or clinical experience
- Apply as soon as possible due to limited time availability
Important Dates
- Application Deadline: March 24, 2026
- Early applications are strongly recommended due to limited vacancies
Why Apply for This Pharma Job?
This role offers a strong foundation for candidates aspiring to build a career in pharmacovigilance and drug safety. You will gain:
- Practical exposure to real-world safety data processing
- Experience with global regulatory standards
- Opportunity to work with a reputed international CRO
- Skill development in clinical safety systems and reporting
- Career growth in a high-demand domain within the pharmaceutical industry
For freshers, this is a valuable entry point into clinical research, while experienced professionals can enhance their expertise in safety operations.
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform. We do not have any direct or indirect association with Fortrea or any recruiter. We do not charge any fees for job postings or applications. Candidates are advised to verify all details on the official company website before applying.
Final Call-to-Action
If you are passionate about pharmacovigilance and want to work in a global clinical research environment, do not miss this opportunity. Apply now before the deadline and take the next step toward a successful pharma career.
