Hiring: Clinical Trial Manager Company: Verastem Oncology Location: Greater Boston Job Posted Time: 2026-09-10 11:46:20 Employment Type: Contract Target Skills & Keywords : GCP, Project Management, Quality Assurance About the job 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. •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. Required Skills: •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. 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 including vendor performance, internal metrics, quality assurance checks and communication of trial status. •Interface directly with Senior Clinical Operations member on RFPs for distribution to vendors, review proposals, coordinate bid defenses and internal discussions in selecting vendors to maximize savings. •Negotiate master service agreements, work orders, contracts, and amendments for sites/vendors. •Assist in developing study-specific feasibilities and participate in site selection. •Contribute to the writing and/or review of clinical documents such as Protocols, Informed Consent Forms, case report forms (CRFs) design and completion guidelines, and other study-related documents. •Work closely with Data Management to ensure ongoing data cleaning including review of data management metric, review of patient profiles and data listings. Qualifications: •Global Phase 3 clinical trial management experience •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. •Demonstrated capacity to prioritize and multi- task. Compensation: •$100,000 - $125,000 / year •Competitive benefits and rewards package Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!