Associate Director, Clinical Trial Management

Summit Therapeutics, Inc.; Menlo Park (CA); On-site; USD 170,000 - 200,000; Full time

Job summary

A leading biotech company based in Menlo Park seeks an Associate Director for Clinical Trial Management. This individual will oversee all aspects of clinical trials, ensuring quality and compliance while managing relationships with vendors and cross-functional teams. Ideal candidates will have extensive experience in managing complex studies and a strong foundation in regulatory standards.

Benefits

Bonuses

Stock options

Health insurance

Qualifications

• 10+ years of clinical project management experience.
• 4+ years in Phase II/III trials.
• Strong knowledge of GCP and regulatory standards.

Responsibilities

• Oversee study scope, quality, timelines, and budget.
• Develop relationships with key opinion leaders.
• Manage clinical trial documents and protocols.

Skills

Clinical project management

Knowledge of drug development

Regulatory standards

Team leadership

Relationship building

Education

Bachelor’s degree in life sciences

Advanced degree preferred

Job description

Associate Director, Clinical Trial Management

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Summit Therapeutics, Inc. provided pay range

This range is provided by Summit Therapeutics, Inc.. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$170,000.00/yr - $200,000.00/yr

Location

On-Site 4 days per week at our Menlo Park, CA office

Overview of Role

The Associate Director, Clinical Trial Management is responsible for all aspects of Clinical Trial Management for global studies, from startup to closeout. This includes coordinating cross-functional teams, managing vendors, and ensuring quality and compliance in line with GCP and regulatory standards.

Responsibilities

• Oversee study scope, quality, timelines, and budget with internal teams, CROs, and vendors.
• Develop and maintain relationships with key opinion leaders and clinical site staff.
• Partner with CROs for patient enrollment and data monitoring strategies.
• Manage clinical trial documents and plans, including protocols, CRFs, and analysis plans.
• Review and approve essential documents and study reports.
• Ensure study compliance with regulatory requirements and company SOPs.
• Oversee the training and performance of clinical staff and CROs.
• Ensure study readiness for inspections and audits.

Qualifications

• Bachelor’s degree in life sciences or related field; advanced degree preferred.
• 10+ years of clinical project management experience, including 4+ years in Phase II/III trials.
• Strong knowledge of drug development, GCP, and regulatory standards.
• Experience managing large, complex studies and budgets.
• Ability to lead teams, build relationships, and work collaboratively.
• Willingness to travel internationally (up to 20%).

Additional Information

The pay range for this role is $168,500 to $198,500 annually, with actual compensation based on experience and other factors. Benefits may include bonuses, stock options, and health insurance.

Employment Details

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Research

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