A Clinical Trial Manager is responsible for planning and managing all aspects of an organization's program of clinical trials, usually for an organization undertaking pharmacological drug testing.
Clinical Trial Manager
in South San Francisco, California
Overview Clinical Trial Manager W2
Contract Pay Rate:
$66 - $76 per hour
Location:
South San Francisco, CA -
Remote Role Job Summary:
Drives the operational execution of assigned clinical studies from study start-up through closeout to ensure delivery of quality clinical data within established timelines and budgets. Partners cross-functionally with Clinical Operations, Data Management, Biostatistics, Medical, Regulatory, and external vendors to support efficient study conduct and regulatory compliance. Applies clinical trial management expertise to resolve operational issues, manage vendors, and ensure adherence to ICH/GCP guidelines, company SOPs, and applicable regulatory requirements. Contributes to continuous improvement initiatives that enhance study execution and operational effectiveness.
Duties and Responsibilities:
Manage day-to-day operational execution of assigned clinical studies to achieve study milestones, quality expectations, and budget objectives.
May lead cross-functional study team activities and coordinate operational deliverables across internal stakeholders and external vendors.
Oversee CROs and study vendors to ensure timely delivery, issue resolution, quality performance, and compliance with study requirements.
Support study start-up activities, including feasibility assessments, country and site selection, vendor selection, system set-up, and user acceptance testing.
Develop and maintain study management plans, operational timelines, and study tracking tools to support effective trial execution.
Ensure inspection readiness and maintain Trial Master File documentation in compliance with ICH/GCP guidelines and company SOPs.
Monitor study progress, identify operational risks, and implement mitigation plans to address issues impacting quality, timelines, or budget.
Contribute to data review, data cleaning activities, and operational review of study outputs and clinical study documentation.
Prepare and review study-related materials, including training content, operational manuals, presentations, and status reports.
Review study invoices, support accrual tracking activities, and monitor study spend against approved budgets.
Requirements and Qualifications:
Typically requires a bachelor's degree in life sciences, nursing, health sciences, or a related field; advanced degree, RN, or PA credentials preferred.
Typically requires 5+ years of clinical research or pharmaceutical industry experience, including 2+ years of clinical trial management experience.
Experience managing global or multi-site clinical studies within a sponsor or CRO environment preferred.
Working knowledge of ICH/GCP guidelines, FDA regulations, and clinical trial processes across study start-up, conduct, and closeout.
Demonstrated ability to manage multiple priorities, solve operational issues, and drive projects independently in a fast-paced environment.
Strong organizational, communication, and cross-functional collaboration skills.
Proficiency with clinical trial systems, study tracking tools, and vendor management processes. Bayside Solutions, Inc. is not able to sponsor any candidates at this time. Additionally, candidates for this position must qualify as a W2 candidate. Bayside Solutions, Inc. may collect your personal information during the position application process. Please reference Bayside Solutions, Inc.'s
