Clinical Trail Manager, Clinical Operations

$125,886 - $175,816/Yr

Cytomx Therapeutics - South San Francisco, CA

Full-time - Senior

Hybrid - South San Francisco, CA

Administrative and Support Services

About the position

The Clinical Trial Manager at CytomX Therapeutics is responsible for providing operational and scientific support for clinical studies, ensuring the execution of clinical strategies, and collaborating with various teams to manage clinical trial activities effectively. This role requires strong organizational skills and the ability to anticipate potential study problems while preparing contingency plans. The Clinical Trial Manager will work closely with study teams and vendors to develop study documents and ensure compliance with clinical monitoring plans, ultimately contributing to the advancement of innovative cancer therapies.

Responsibilities

• Develop and manage the execution of clinical trial operational activities to ensure completion according to timelines.
• Work directly with study team and/or vendors on development of study documents, plans, and manuals.
• Develop and ensure compliance with clinical monitoring plan and associated key performance indicators (KPIs).
• Review monitoring trip reports and ensure accurate identification, tracking, and resolution of all protocol deviations and action items.
• Collaborate with the clinical development team to ensure appropriate data review and accurate data reporting.
• Procure and manage contracts with CROs, study vendors, and investigative sites.
• Provide vendor oversight of assigned clinical trial vendors.
• Review and approve vendor and investigative site invoices.
• Manage study-wide activities such as sample handling, drug re-supply, and investigator payments.
• Provide frequent study updates to management upon request.
• Ensure trial activities are documented in the trial master file in accordance with regulatory requirements and SOPs.
• Collaborate cross-functionally in the preparation of scientific publications including posters, abstracts, and manuscripts.
• Support the implementation of new clinical SOPs, systems, and processes.
• May mentor, manage, and develop other team members.

Requirements

• A minimum of a Bachelor's degree in clinical, biological, mathematical sciences or related field is required; an advanced degree is preferred.
• A minimum of 5 years pharmaceutical development experience is strongly preferred.
• Demonstrated problem-solving abilities and strong organizational skills.
• Excellent written and verbal communication skills are required.
• Experience and understanding of ICH and GCP is preferred.
• Demonstrated self-starter and team player with strong interpersonal skills.

Nice-to-haves

• Experience in managing clinical trials in a pharmaceutical setting.
• Familiarity with regulatory requirements and compliance in clinical research.

Benefits

• Competitive salary range of $125,886 - $175,816 per year.
• Robust and highly competitive total rewards program.
• Strong learning curriculum and career guidance for development and growth.
• Collaborative work environment that promotes teamwork and shared vision.