Fortrea Hiring Safety Science Coordinator for Freshers

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Fortrea Hiring Safety Science Coordinator for Freshers


Fortrea, a global leader in clinical research and drug safety, has announced a new opportunity for the role of Safety Science Coordinator I at its Pune office. This opening is an excellent chance for professionals in pharmacovigilance or clinical safety who are looking to expand their careers in a globally recognized Contract Research Organization (CRO). Fortrea Hiring Safety Science Coordinator

In this article, we provide complete information about the job responsibilities, required qualifications, skills, experience, and how to apply for this exciting opportunity.


About Fortrea

Fortrea is a prominent global Contract Research Organization (CRO) that delivers end-to-end solutions across the drug development lifecycle. With decades of experience in clinical trials, regulatory submissions, and pharmacovigilance, Fortrea partners with pharmaceutical, biotechnology, and medical device companies to ensure that patient safety and data accuracy remain a top priority.

The organization is known for maintaining high-quality standards, strict regulatory compliance, and global operational reach. Fortrea’s team includes experts from medical, pharmaceutical, and scientific backgrounds, delivering innovative approaches to support clinical and safety operations.


Job Location and Employment Type

  • Position: Safety Science Coordinator I
  • Location: Pune, Maharashtra
  • Job Type: Full-time, On-site
  • Job ID: 253901

This role is based in Fortrea’s Pune facility, offering a collaborative work environment with exposure to international pharmacovigilance standards. Fortrea Hiring Safety Science Coordinator


Key Responsibilities

Candidates selected for the Safety Science Coordinator I position will have the following responsibilities:

1. Expedited and Periodic Safety Reporting

  • Process Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs).
  • Maintain accurate and updated tracking of adverse events.
  • Ensure timely submission of safety reports to global regulatory authorities such as the FDA, EMA, and others.
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2. Adverse Event (AE/SAE) Management

  • Record and manage Adverse Events (AEs) and Serious Adverse Events (SAEs).
  • Perform MedDRA coding, narrative writing, and assess listedness of events (especially for marketed products).
  • Ensure data entry is accurate and timely across safety systems.

3. Regulatory and Compliance Support

  • Ensure full compliance with ICH-GCP, local regulations, and global pharmacovigilance requirements.
  • Participate in database reconciliation, audit preparedness, and internal quality checks.
  • Support documentation and ensure that SOPs are followed.

4. Team Collaboration and Training

  • Coordinate with cross-functional teams, including clinical operations, data management, and regulatory affairs.
  • Provide mentoring and peer-review support to junior team members.
  • Contribute to internal training and quality improvement initiatives.

5. Administrative and Documentation Tasks

  • Manage safety-related documentation and maintain trial master files.
  • Schedule and facilitate team meetings.
  • Assist in maintaining audit-ready safety documentation systems.

Eligibility Criteria

Educational Qualifications

Candidates must hold one of the following degrees:

  • PharmD / M.Pharm / B.Pharm (Preferred)
  • Graduates in Nursing, Medicine, or Life Sciences with relevant pharmacovigilance experience are also eligible to apply.

Work Experience

Applicants should have:

  • A minimum of 2 years of experience in pharmacovigilance, clinical safety, or clinical research.
  • Strong background in AE/SAE reporting, safety database management, and MedDRA coding.
  • Experience in working with CROs, pharmaceutical, or biotech companies is a plus. Fortrea Hiring Safety Science Coordinator

Skills Required

To be successful in this role, candidates must demonstrate:

  • Strong attention to detail and analytical thinking.
  • High level of proficiency in MS Office tools and pharmacovigilance databases.
  • Excellent verbal and written communication skills in English.
  • Ability to multi-task, meet deadlines, and manage responsibilities independently or as part of a team.
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Benefits and Growth Opportunities

Fortrea offers a structured and professional work environment where employees can grow both technically and professionally.

Some of the key benefits include:

  • Competitive Salary Package
  • Opportunities for global exposure in pharmacovigilance and safety science
  • Structured training programs and mentoring from senior professionals
  • Work in a collaborative and diverse team
  • Access to the latest tools and technologies used in global safety reporting

Why Join Fortrea?

Fortrea has earned a reputation as one of the top CROs globally, with a consistent track record of successful clinical and post-market safety projects. By joining the Fortrea team, candidates will be part of a purpose-driven company focused on patient safety, regulatory compliance, and scientific excellence. Fortrea Hiring Safety Science Coordinator

With continuous learning opportunities, access to a global talent network, and a strong focus on employee development, Fortrea offers an ideal platform for pharmacovigilance professionals to advance their careers.


How to Apply?

Candidates interested in applying for the Safety Science Coordinator I position in Pune can follow the steps below:

  1. Visit Fortrea’s official careers page or apply through trusted job portals.
  2. Search for Job ID: 253901.
  3. Submit your updated resume and relevant documents.
  4. Ensure you meet the experience and qualification requirements before submitting the application.

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Final Thoughts

The Safety Science Coordinator I role at Fortrea is a promising opportunity for professionals who are passionate about pharmacovigilance, regulatory safety, and global clinical compliance. With a minimum of two years of experience and a relevant educational background, this job can be a stepping stone to more advanced roles in drug safety and clinical research.

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If you are ready to contribute to global healthcare by ensuring safety and compliance in drug development, this role at Fortrea in Pune may be the ideal next step in your career. Fortrea Hiring Safety Science Coordinator


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