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Safety Science Analyst

2+ years
Not Disclosed
10 March 19, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Clinical Safety Associate

Company: Fortrea, a Global Contract Research Organization (CRO)

Location: [Insert Location]


Job Overview:

Fortrea is seeking a Clinical Safety Associate to support the overall Clinical Safety and/or Post-Marketing Surveillance (PSS) operations related to products, including the complete adverse events process. This may involve safety data collected from clinical trials and post-marketing settings (e.g., unsolicited reports). The Clinical Safety Associate will manage and process expeditable adverse events, ensuring they meet required standards and are submitted to clients and/or regulatory agencies within agreed timelines.

This role will involve delivering high-quality service to both internal and external clients, ensuring safety data is processed in a safe and cost-effective manner while complying with legal requirements.


Key Responsibilities:

  • Assist with clinical safety operations, including managing adverse event data from clinical trials and post-marketing settings.
  • Process and manage expeditable adverse events to the required standards and ensure submission to clients or regulatory agencies within stipulated timelines.
  • Provide support to client project groups or offer standalone services, ensuring all clients receive the appropriate quality of service.
  • Comply with legal requirements of the Health and Safety at Work Act 1974, COSHH regulations 1989, and the EC Directives 1992/3 as outlined in the company’s Health and Safety Manual.

Why Join Fortrea?

Fortrea offers a dynamic and collaborative environment where professionals can thrive and contribute to the revolution of drug and device development. Join us to make a global impact and be part of an inclusive, diverse team.


Fortrea is an Equal Opportunity Employer:

As an EOE/AA employer, Fortrea promotes diversity and inclusion in the workplace and does not tolerate harassment or discrimination. We make employment decisions based on business needs and individual qualifications without regard to race, religion, color, national origin, gender, sexual orientation, age, veteran status, disability, or any other legally protected characteristic.

For more information about how we collect and store your personal data, please see our Privacy Statement.

If you require a reasonable accommodation for the application process or interviews due to a disability, please contact: taaccommodationsrequest@fortrea.com.