Clinical Trial Manager

Verastem Oncology

Clinical Trial Manager overseeing global Phase 3 clinical trials for Verastem Oncology. Leading project teams, vendor management, and compliance with regulatory requirements in a hybrid role.

Posted 8/2/2026full-timeBoston • Massachusetts • 🇺🇸 United StatesMid-LevelSenior💰 $100,000 - $125,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing global Phase 3 clinical trials, ensuring compliance with ICH and GCP guidelines, and effectively liaising with clinical vendors and cross-functional teams. Proficient in contract negotiation and oversight of project lifecycles from initiation to closeout.

Highest-signal resume keywords

Global Phase 3 Clinical Trial ManagementOncology Clinical Studies ExperienceICH and GCP Regulatory KnowledgeContract NegotiationProject Lifecycle Oversight

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementRegulatory ComplianceData ManagementSOP AdherenceFeasibility Development

Soft Skills

Verbal CommunicationWritten CommunicationPrioritizationMulti-tasking

Tools & Technologies

CROIRTETMF

Industry Keywords

Clinical TrialsOncologySOW ManagementVendor LiaisonMonitoring Activities

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Function as primary liaison between clinical vendors (CRO, IRT, eTMF) and Verastem Oncology
Proactively recognize any changes in SOW and work with CRO to manage accruals and SOW changes
Manage assigned clinical trials to ensure that studies are conducted efficiently, on time, within budget and in accordance with established SOPs and applicable regulatory requirements
Provide oversight of all elements of the project lifecycle from initial set-up to close out
Work with Senior Clinical Operations member on RFPs for distribution to vendors
Negotiate master service agreements, work orders, contracts, and amendments for sites/vendors
Assist in developing study-specific feasibilities and participate in site selection
Liaise with medical monitor and cross functional team members
Work closely with Data Management to ensure ongoing data cleaning
Oversee monitoring activities at clinical CROs by reviewing monitoring visit reports

Requirements

What you’ll need

Global Phase 3 clinical trial management experience
Minimum of 3 years of clinical trial experience, including prior experience in oncology clinical studies
BA/BS degree or equivalent in a scientific or health care field is required
Excellent understanding of ICH, GCP and other applicable regulatory guidelines required
Excellent verbal and written communication skills to effectively communicate with site staff, vendors and internal cross functional team members
Ability to prioritize and multi-task
Travel may be required

Benefits

Comp & perks

Eligible for an annual bonus
Equity compensation
Competitive benefits package