Clinical Study Manager

Get AI‑powered advice on this job and more exclusive features. Rochester Clinical Research provided pay range This range is provided by Rochester Clinical Research. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $90,000.00/yr - $95,000.00/yr Job Summary The Clinical Site Manager is responsible for the overall management of the life of a clinical trial, overseeing the work of Study Coordinators and Clinical Research Nurses to ensure efficiency and success of the applicable trial. Key Responsibilities Team Leadership and Coordination Supervise and mentor Study Coordinators and Clinical Research Nurses Provide training and ensure all staff is familiar with the study protocol, ethical guidelines, and safety requirements Foster effective communication among all stakeholders Clinical Responsibilities Be the expert on assigned trials; understanding and implementing the protocol. Create study timelines and execution planning (IP delivery, lab kits, etc) Involved in all study planning - monitor communications, attending IM + SIV, approving source creation (paper and electronic) Be able to act as the backup to the coordinators Serve as primary escalation and contact for resolution of issues that arise throughout trial for both internal and external teams Regulatory Responsibilities Managing internal greenlight process - ensuring all training and delegations are appropriately signed and completed, collaborating with regulatory Maintain all appropriate documentation throughout the trial Ensure all invoiceables are captured correctly for studies Work with QA to evaluate root‑cause analysis of CAPA’s Educational Responsibilities Collaborate with new clinical staff to ensure adequate development of CRN’s/SC’s Be a resource and educator for all coordinators Qualifications Strong team leadership and management skills Strong verbal and written communication skills Strong interpersonal and customer service skills Strong organizational skills and attention to detail Strong time management skills with a proven ability to meet deadlines Strong analytical and problem‑solving skills Ability to prioritize tasks and to delegate them when appropriate Ability to function well in a high‑paced environment Education and Experience Bachelor's or Associates degree in health or science related field required BSN Preferred 3-5 years of experience in clinical research, with at least 2 years in a managerial role overseeing clinical studies or trials Seniority level Associate Employment type Full‑time Job function Research and Management Benefits Medical insurance Vision insurance 401(k) Disability insurance #J-18808-Ljbffr