Job Summary : Responsibilities :

• Working closely with the Clinical Safety Manager to ensure each project deliverables are met;
  
• Collect, process, and track serious adverse event (SAE) reports and clinical event documents;
  
• Generate and track study report safety narratives;
  
• Coordinate safety surveillance activities (e.g., lab review and trend analysis);
  
• Generate Investigator Safety Letters and distribution to health authority;
  
• Assist in preparation of clinical safety documents
  
• Perform safety submissions of expedited/periodic reports in Singapore/Taiwan/China

Qualifications :

• Bachelor’s degree in health/life sciences with 2-4 years of clinical trial safety or Pharmacovigilance experience ;
  
• Proficient in a range of Clinical Safety tasks, as detailed in the ‘responsibilities’ section (above)
  
• Excellent time management skills with an ability to work on tight timelines;
  
• An ability to interact well within a team environment, but also work independently and manage own workload;
  
• Proficient in Microsoft Office and demonstrated ability to efficiently use safety database;
  
• Strong attention to detail;
  
• Demonstrate comprehensive knowledge of Good Clinical Practice (GCP) guidelines
  

Medpace Overview : Why Medpace? :
Medpace Perks

• Hybrid work-from-home options (dependent upon position and level)
• Competitive PTO packages
• Employee health and wellness initiatives
• Flexible work schedule
• Competitive compensation and benefits package
• Structured career paths with opportunities for professional growth

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility