Senior Clinical Trial Manager

6+ years

$154,000 - $175,000 per year

San Mateo

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.

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Senior Clinical Trial Manager

Job Description

Job Summary:

Key Responsibilities:

Qualifications:

Desired Skills:

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