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Clinical Safety Coordinator - Pharmacovigilance / Drug Safety

2-4 years
Not Disclosed
10 Jan. 13, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Clinical Safety Coordinator

Location: Taiwan Office
Company: Medpace


Job Summary

We are seeking a full-time, office-based Clinical Safety Coordinator to join our team in Taiwan. This role is essential to the success of our projects and company objectives. If you’re looking for an exciting career where you can utilize your expertise, develop new skills, and grow professionally, this opportunity is for you.


Responsibilities

  • Collaborate with the Clinical Safety Manager to meet project deliverables.
  • Collect, process, and track serious adverse event (SAE) reports and clinical event documents.
  • Generate and monitor study report safety narratives.
  • Coordinate safety surveillance activities, including lab review and trend analysis.
  • Prepare and distribute Investigator Safety Letters to health authorities.
  • Assist in preparing clinical safety documents.
  • Perform safety submissions for expedited/periodic reports in Singapore, Taiwan, and China.

Qualifications

  • Bachelor’s degree in health or life sciences with 2–4 years of clinical trial safety or pharmacovigilance experience.
  • Proficient in clinical safety tasks as outlined in the responsibilities above.
  • Strong time management skills, with the ability to work under tight timelines.
  • Team player with the ability to work independently and manage personal workload effectively.
  • Proficient in Microsoft Office and experienced with safety databases.
  • Excellent attention to detail.
  • Comprehensive knowledge of Good Clinical Practice (GCP) guidelines.

About Medpace

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through scientific and disciplined approaches.


Why Join Medpace?

People. Purpose. Passion.

At Medpace, we strive to make a meaningful difference in the lives of patients worldwide.

Benefits and Perks:

  • Flexible work environment
  • Competitive compensation and PTO packages
  • Structured career growth opportunities
  • Employee health and wellness initiatives
  • Company-sponsored appreciation events

Awards and Recognition

  • Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024).
  • Recipient of CRO Leadership Awards for expertise, quality, and reliability.

What to Expect Next

If your qualifications match the role, a Medpace team member will contact you with details about the next steps.

Apply Today to join Medpace and contribute to life-changing medical advancements.

Medpace is an Equal Opportunity Employer. We welcome applications from individuals of all backgrounds, including veterans and persons with disabilities.