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Clinical Trial Manager

3+ years
Not Disclosed
10 Nov. 27, 2024
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

About the Job
Title: Clinical Trial Manager
Location: Foster City, CA (100% onsite)
Duration: 6–12 months

Responsibilities:

  • Collaborate with the Project Manager to set targets for the clinical monitoring team and ensure trial recordings align with project goals.
  • Create and implement study-specific clinical monitoring tools and documentation.
  • Develop and oversee the trial budget.
  • Identify, recruit, and select clinical trial sites, coordinating site management activities.
  • Supervise and coordinate the clinical monitoring team.
  • Provide project-specific training to Clinical Research Associates and conduct regular meetings with them.
  • Record and communicate client interactions, acting as their representative.
  • Plan and manage site visits.
  • Collect and review trial documents.
  • Ensure compliance with SOPs, local regulations, and industry standards including CFR, ICH, and GCP guidelines.