Sr. CLINICAL TRIAL MANAGER (Contract)

BS or higher degree in science, nursing (RN or BSN), or equivalent discipline

A minimum of 7 years of clinical research experience in biotechnology, pharmaceutical, or CRO industry

Experience supporting studies in a fast-paced environment

Success in working with CROs and vendors

Excellent communication skills and ability to achieve milestones in a team environment

Strong working knowledge of FDA, ICH Guidelines, and GCPs governing the conduct of clinical trials

$80

—

$130 USD

Adicet fosters a collaborative, high-performing environment by prioritizing in-person engagement. To enhance teamwork and communication, employees are required to be onsite

at least three days per week (Tuesday–Thursday mandatory)

, with some roles requiring full-time onsite presence.

Ensure clinical trial activities and deliverables are completed on-time, within budget, and in a complex environment in accordance with quality and GCP standards with minimal oversight

Lead the identification, evaluation, selection, and oversight of clinical trial sites, vendors and CROs

Work closely with the Clinical Operations team to support all aspects of clinical studies

Manage multiple clinical study vendors with oversight of activities.

Plan and conduct Investigator’s meetings

Take a leadership role in certain site and study management activities including: ICFs, site activations, monitoring reports and study plans