Clinical Trial Associate

One of our clients is looking for a Clinical Trial Management Associate (CTMA) to support the successful execution of their clinical trials. In this key role, you will partner closely with the Clinical Trial Manager (CTM) and Director, Clinical Operations to manage critical components of study delivery—ensuring timelines, quality standards, and budget expectations are met. You will drive meeting coordination, site and vendor support, documentation management, and quality oversight across assigned studies. Requirements: • Bachelor’s degree in health sciences or equivalent. • 3+ years of experience in working on phase I-IV global clinical studies within a biopharmaceutical/biotech, CRO, or academic environment. • Oncology experience required. Prostate cancer experience highly preferred. • Experience and understanding of global clinical trial operations; preference in the oncology and/or cell therapy space • Current knowledge of Good Clinical Practices, ICH Guidelines, and FDA regulations and the application of the conduct to clinical studies. • Ability to interpret and communicate protocol requirements. • Demonstrated experience managing components of clinical trials independently. • Advanced proficiency with clinical trial software platforms, vendor systems, and related tools. • Understanding of data-technology interdependencies, vendor metrics, and operational nuances across vendor types. • Ability to interface with medical personnel at clinical site(s) and support multi-disciplinary teams both internally and externally. • Must be proficient in MS Office Suite (Word, Excel, PowerPoint) and project management programs. • Excellent communication skills. Ability to communicate in an open, clear, timely and consistent manner. • Ability to contribute as a team member in a dynamic, fast-paced biotech environment. • The candidate must reside in the Greater Boston area. • 10% to 20% travel required.