Fortrea Hiring Pharmacovigilance Safety Science Coordinator II

Fortrea Hiring Safety Science Coordinator II for Pharmacovigilance Team in Pune

Fortrea, a global clinical research organization, has announced hiring for the position of Safety Science Coordinator II in Pune. This opportunity is significant for B.Pharm, M.Pharm, PharmD, and life science graduates who want to build careers in pharmacovigilance, drug safety, and clinical research safety monitoring.

End Date: March 10, 2026 (3 hours left to apply)

As pharmaceutical companies continue expanding global clinical trials and post‑marketing drug surveillance programs, safety science roles are becoming increasingly important. Professionals in these positions ensure that adverse events and patient safety data collected during clinical trials are accurately processed, reviewed, and reported to regulatory authorities.

For graduates interested in entering the fast‑growing pharmacovigilance and drug safety sector, this role provides valuable exposure to global safety databases, regulatory reporting standards, and international clinical trial safety monitoring systems.

Company Overview

Fortrea is a global contract research organization specializing in clinical development, pharmacovigilance, and regulatory services for pharmaceutical and biotechnology companies. The organization works with sponsors worldwide to manage clinical trials, drug safety monitoring, regulatory submissions, and post‑marketing surveillance activities.

Through advanced clinical research infrastructure and regulatory expertise, Fortrea supports pharmaceutical companies in bringing innovative medicines to market while ensuring patient safety and regulatory compliance.

Fortrea’s pharmacovigilance and safety science teams play a vital role in monitoring adverse events reported during clinical trials and post‑marketing studies. These teams help ensure that medicines meet global safety standards required by regulatory agencies such as the US FDA, EMA, and other international authorities.

Career Outlook for Safety Science Analysts in 2026

The pharmacovigilance and drug safety sector is expected to grow rapidly through 2026 as regulatory agencies worldwide strengthen safety monitoring requirements for pharmaceutical products. Pharmaceutical companies and CROs are investing heavily in safety data management systems and adverse event monitoring infrastructure.

Safety science professionals are responsible for identifying, evaluating, and reporting potential safety risks associated with medicines. Their work ensures that patients participating in clinical trials or using approved medicines are protected through continuous safety monitoring.

Professionals entering the safety science field often progress into roles such as Drug Safety Associate, Pharmacovigilance Specialist, Medical Safety Reviewer, Safety Scientist, or Global Pharmacovigilance Manager. With increasing regulatory scrutiny and growing volumes of clinical safety data, pharmacovigilance professionals will remain highly valuable in the pharmaceutical industry.

Job Role & Responsibilities

The Safety Science Coordinator II will support pharmacovigilance operations by managing adverse event reports and ensuring regulatory compliant safety data processing.

Key responsibilities include:

• Process adverse event reports collected from clinical trials and post‑marketing sources
• Enter safety data into pharmacovigilance databases and tracking systems
• Review adverse event reports for completeness, accuracy, and regulatory compliance
• Write patient narratives describing clinical safety cases
• Code adverse events using standardized medical dictionaries such as MedDRA
• Identify missing clinical information and generate follow‑up queries
• Ensure cases receive appropriate medical review and validation
• Prepare and submit expedited safety reports to regulatory authorities
• Support periodic safety report preparation and submission
• Maintain project documentation and pharmacovigilance tracking systems

These responsibilities ensure that clinical safety information is handled accurately and submitted within strict regulatory timelines.

Regulatory Compliance & Documentation

Professionals in this role must ensure all pharmacovigilance activities comply with international regulatory standards.

Key compliance responsibilities include:

• Maintain compliance with Good Clinical Practice and pharmacovigilance regulations
• Follow standard operating procedures and work instructions for safety reporting
• Maintain accurate safety databases and case documentation
• Support regulatory inspections and internal quality audits
• Assist in database reconciliation and project documentation activities

Maintaining regulatory‑compliant documentation is essential for ensuring transparency and patient safety during clinical trials.

Eligibility / Qualifications

Candidates applying for this pharmacovigilance opportunity should meet the following criteria:

• Degree in Pharmacy, Biological Sciences, Nursing, Medical Sciences, or related life science discipline
• Bachelor’s, Master’s, or PharmD degree with at least one year of relevant safety or clinical research experience
• Strong understanding of pharmacovigilance processes and adverse event reporting
• Knowledge of clinical trial safety monitoring and regulatory reporting requirements
• Strong analytical and organizational skills

Relevant education backgrounds may include: B.Pharm, M.Pharm, PharmD, B.Sc Life Sciences, B.Sc Biotechnology, B.Sc Microbiology, M.Sc Clinical Research, M.Sc Biotechnology.

Skills & Competencies

Candidates should demonstrate the following abilities:

• Strong attention to detail and high accuracy in data processing
• Ability to work collaboratively with pharmacovigilance teams
• Good written and verbal communication skills
• Knowledge of MS Office and safety database systems
• Ability to manage multiple safety cases within strict timelines

Mentoring ability and experience supporting pharmacovigilance teams may be considered an advantage.

Location & Salary

Location: Pune, Maharashtra, India

Work Model: Office environment with possible remote flexibility depending on project requirements.

Application Process

Interested candidates can apply through the official Fortrea careers portal using the link below.

Apply here:
https://fortrea.wd1.myworkdayjobs.com/Fortrea/job/Pune/Safety-Science-Coordinator-II_26491

Applicants should submit an updated resume highlighting experience in pharmacovigilance, adverse event processing, safety databases, and clinical trial safety monitoring.

Early application is recommended as pharmacovigilance positions in leading CRO organizations often receive strong interest from qualified candidates.

Frequently Asked Questions

Who can apply for the Fortrea Safety Science Coordinator role?
Candidates with degrees in pharmacy, biological sciences, medical sciences, nursing, or related life science fields with relevant safety experience can apply.

What does a safety science coordinator do?
Safety science professionals process adverse event reports, maintain safety databases, and ensure drug safety information is reported to regulatory authorities.

Is pharmacovigilance experience required for this role?
Yes. Candidates typically require at least one year of relevant safety or clinical research experience.

What career growth opportunities exist in pharmacovigilance?
Professionals can advance into roles such as Drug Safety Associate, Pharmacovigilance Specialist, Medical Safety Reviewer, or Global Safety Scientist.

Summary

Category	Details
Company	Fortrea
Vacancies	Safety Science Coordinator II
Required Education	B.Pharm, M.Pharm, PharmD, B.Sc Life Sciences, M.Sc Biotechnology
Experience	Minimum 1 year in pharmacovigilance or clinical safety
Location	Pune, Maharashtra
Department	Pharmacovigilance / Safety Science

Tagged as: pharma jobs in pune