Clinical Trial Manager

Job Summary

C4 Therapeutics is seeking an initiative-taking Clinical Operations professional to lead the successful execution of assigned clinical trial(s) in oncology from First in Human through Phase III. The Clinical Trial Manager will be responsible and accountable for planning and execution of day-to-day study operations including leading the cross-functional study core team, representing C4T in CRO study team meetings (and being accountable for adherence with overall clinical trial timelines, budget, quality, and regulatory standards (ICH/GCP, internal SOPs)). This is a hybrid role with expected regular presence at our Watertown, MA office.

About C4 Therapeutics

C4 Therapeutics (C4T) (Nasdaq: CCCC) is a clinical-stage biopharmaceutical company dedicated to delivering on the promise of targeted protein degradation science to create a new generation of medicines that transforms patients’ lives. C4T is progressing targeted oncology programs through clinical studies and leveraging its TORPEDO® platform to efficiently design and optimize small-molecule medicines to address difficult-to-treat diseases. C4T’s degrader medicines are designed to harness the body’s natural protein recycling system to rapidly degrade disease-causing proteins, offering the potential to overcome drug resistance, drug undruggable targets and improve patient outcomes. For more information, please visit www.c4therapeutics.com.

Required

• A Bachelor’s Degree in health/life sciences or related field, with a minimum of five years of progressive clinical operations experience, including trial management across phases of development at a pharmaceutical or biotechnology sponsor, serving as a primary point of contact for CROs and third-party vendors.
• Demonstrated knowledge of clinical operations methodologies, FDA Regulations, ICH/GCP guidelines in clinical trials, and related organizational, project management, and leadership capabilities.
• Demonstrated experience with contributing to clinical operations strategy and developing and/or inputting into key clinical trial plans.
• Ability to communicate and collaborate in an open and clear manner with varied stakeholders, listening effectively and inviting response and discussion with internal partners and external service providers.
• Demonstrated effective problem-solving, and risk management to prevent and overcome complex safety and compliance related issues during clinical study implementation.

Preferred

• Experience with oncology clinical trial management and/or global clinical trials.

Compensation

The base pay range for this position at commencement of employment is expected to be between $138,566.00 and $153,118.00 annually; however, base pay offered may vary depending on multiple individualized factors, including job-related knowledge, skills, and experience.

Equal Opportunity Employer

C4 Therapeutics is an Equal Opportunity Employer.