A company is looking for a Clinical Research Project Manager I focused on Cutaneous Oncology clinical trials.
Key Responsibilities
Manage daily operations of clinical trials, ensuring compliance and adherence to timelines
Develop and maintain the Trial Master File (TMF) to ensure document compliance with regulatory standards
Assist in the development of protocols and consent forms, ensuring clarity and regulatory compliance
Required Qualifications
Bachelor's degree in a relevant field
Three years of experience in clinical research or project management, preferably in multi-center oncology trials
Experience in an academic institution with clinical trial coordination and management
Basic understanding of clinical trial processes and Good Clinical Practice (GCP) guidelines
Familiarity with trial management software, such as EPIC and OnCore
Clinical Project Manager • Bridgeport, Connecticut, United States