Global Phase 3 Clinical Trial Lead

Verastem Oncology; Massachusetts; On-site; USD 100,000 - 125,000; Full time

Job summary

Verastem Oncology in the United States seeks a Clinical Trial Manager with global Phase 3 experience to lead cross-functional teams, oversee CROs and ancillary vendors, and ensure timely, budget-conscious delivery of trial milestones.

You will drive study setup, execution, and closeout while maintaining GCP/SOP compliance, risk management, and quality standards across multiple vendors and sites.

Qualifications

• Global Phase 3 clinical trial management experience.
• Minimum of 3 years of clinical trial experience, including oncology.
• BA/BS degree or equivalent in a scientific or health care field.

Responsibilities

• Function as primary liaison between clinical vendors (CRO, IRT, eTMF) and Verastem Oncology to ensure understanding of expectations and scope of work, quality and budget.
• Manage assigned clinical trials to ensure that studies are conducted efficiently, on time, within budget and in accordance with SOPs and regulatory requirements.
• Provide oversight of all elements of the project lifecycle from setup to closeout, including vendor performance and quality checks.
• Coordinate vendor selection activities, review proposals, and participate in bid defenses to maximize savings.
• Negotiate master service agreements, work orders, contracts, and amendments for sites/vendors.
• Assist in feasibility studies and site selection for trials.
• Contribute to writing and review of clinical documents (protocols, CRFs, ICF templates).
• Collaborate with data management, QA, and medical monitoring to ensure audit readiness.

Skills

Phase 3 management

Oncology experience

Regulatory knowledge

Education

BA/BS in science or health care

Job description

Verastem Oncology in the United States seeks a Clinical Trial Manager with global Phase 3 experience to lead cross-functional teams, oversee CROs and ancillary vendors, and ensure timely, budget-conscious delivery of trial milestones.

You will drive study setup, execution, and closeout while maintaining GCP/SOP compliance, risk management, and quality standards across multiple vendors and sites.