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Senior Clinical Trial Manager

6+ years
$154,000 - $175,000 per year
10 March 3, 2025
Job Description
Job Type: Full Time Education: BA/BS 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

Senior Clinical Trial Manager – Redwood City, CA

Location: Hybrid (San Mateo County, CA)
Salary Range: $154,000 - $175,000 per year
Employment Type: Full-Time (Direct Hire)
Hourly Rate: $74/hr - $84/hr

Job Summary:

A leading healthcare company is seeking a Senior Clinical Trial Manager to independently manage clinical trials from start-up through database lock. This role will oversee multiple clinical studies, provide operational leadership, and ensure compliance with regulatory guidelines.

Key Responsibilities:

  • Manage all phases of global clinical studies (Phase 1 and beyond).
  • Lead cross-functional teams to achieve study objectives.
  • Act as a global lead for complex studies and oversee study management teams.
  • Ensure proper selection, training, and oversight of investigative sites.
  • Supervise and mentor CTMs, CRAs, and other team members.
  • Partner with outsourcing teams for vendor agreements and site budgets.
  • Manage external vendors and study budgets for cost-effectiveness.
  • Identify risks in clinical studies and implement mitigation strategies.
  • Oversee study timelines, quality metrics, and data integrity.
  • Develop and review clinical trial documents (protocols, CRFs, ICFs, study plans).

Qualifications:

  • Education: BS/BA in Life Science or a related field.
  • Experience:
    • 6+ years in clinical operations or drug development.
    • 2+ years in a sponsor company.
    • 1+ year as a global study lead.
  • Strong knowledge of FDA & ICH/GCP regulations and clinical development processes.
  • Proficiency in Microsoft Office and technical writing.
  • Experience in vendor management, CRO selection, and oversight.
  • Ability to manage multiple studies, collaborate with stakeholders, and influence key decisions.
  • Preferred Experience: Global clinical trials in oncology and/or ophthalmology and early-phase trial management.

Desired Skills:

  • Clinical operations, drug development, regulatory compliance.
  • Strong leadership, communication, and organizational skills.
  • Technical writing experience (clinical protocols, study plans, etc.).
  • Experience in vendor and budget management.

Apply now to join a leading team in clinical research and contribute to innovative healthcare solutions.