Join Cleveland Clinic's Main Campus where research and surgery are advanced, technology is leading-edge, patient care is world class and caregivers are family. Here, you will work alongside a passionate and dedicated team, receive endless support and appreciation, and build a rewarding career with one of the most respected healthcare organizations in the world. As a Clinical Research Project Manager, you will oversee a variety of research projects within the Center for Value Based Care, focusing primarily on the behind-the-scenes work essential to advancing innovative treatments. In this role, you will collaborate with researchers and clinical caregivers, contribute perspective, support budgeting and contracting processes, monitor patient visits, and facilitate day-to-day study operations. This position allows you to support externally funded projects in PCI and contribute to the mission of Cleveland Clinic to create value in healthcare and enhance care delivery, with diverse projects that provide exposure to multiple disciplines across the system. Read more about the Center for Value Based Care: https://my.clevelandclinic.org/departments/community-care/research-innovations/care-research **A caregiver in this role works days from 8:00 a.m. - 5:00 p.m.** **This role is fully on site during the new hire period and transitions to a hybrid schedule after training, typically with two to three days in the office.** **_Occasional travel to regional hospitals and Family Health Centers may be required depending on project needs._** A caregiver who excels in this role will: + Oversee the administrative functions of single and/or multi-institutional research trials. + Coordinate/manage daily organization and operational issues/activities related to Phase I-IV clinical research trials. + Facilitate key trial communications for academic coordination. + Provide clinical perspective to the design and conduct of clinical trials. + Manage and coordinate a clinical trials team (external industry team members, statisticians, database programmers and researchers) responsible for data accumulation, input and analysis. + Interact with the Finance and Legal Departments to facilitate clinical trial budget, site budget and contract execution. + Maintain professional relationships with sponsors, including frequent, open communication and associated documentation. + Coordinate development, preparation, review and approval of research protocols, case report forms and regulatory documents for the conduct of research required by Institutional Review Board (IRB), Sponsor and FDA. + Collect and review regulatory documents from sites. + Communicate with institutional and central IRBs, FDA and other parties regarding protocol subject and safety issues. + Organize, coordinate, attend and participate in Investigator Meetings and training programs. + Develop and maintain planned communication with sites (i.e., newsletters, study progress updates, telephone communication, supportive reinforcement of Sponsor communication, etc.). + Analyze site strengths and weaknesses related to intended protocol and selection of qualified investigators and sites. + Assess investigator and site performance. + Lead initiatives to improve quality and make recommendations to discontinue sites if necessary. + Assist with the development, implementation and evaluation of research subject recruitment strategies, including marketing strategies, to maximize enrollment and retention. + Complete training in Human Subjects Research (HSR) within 90 days or hire. Minimum qualifications for the ideal future caregiver include: + Bachelor's degree in Nursing, Science, Healthcare or Computer Science with an emphasis on programming **and** three years of clinical research experience as a Study Coordinator, Project Manager, Contract Research Associate or equivalent in a related field + **OR** High School Diploma/GED **and** seven years of experience + **OR** Associate's degree **and** five years of experience + **OR** Master's degree **and** two years of experience + Substantial scientific and medical knowledge across relevant therapeutic areas + Demonstrated ability to work with multiple software technologies + Knowledge of FDA regulations, GCPs and internal SOPs + Knowledge of the Code of Federal Regulations, ICH and GCP guidelines and their applications to clinical research trials + Complete training in Human Subjects Research (HSR) within 90 days or hire Preferred qualifications for the ideal future caregiver include: + Society of Clinical Research Associates (SOCRA) or Association of Clinical Research Professionals (ACRP) Certification + Supervisory experience + Familiarity and experience with healthcare operations **Physical Requirements:** + Requires full range of motion, manual and finger dexterity and eye-hand coordination. + Requires standing and walking for extensive periods of time. + Requires normal or corrected hearing and vision to normal range. **Personal Protective Equipment:** + Follows standard precautions using personal protective equipment as required. **Pay Range** Minimum Annual Salary: $63,250.00 Maximum Annual Salary: $96,467.50 The pay range displayed on this job posting reflects the anticipated range for new hires. A successful candidate's actual compensation will be determined after taking factors into consideration such as the candidate's work history, experience, skill set and education. The pay range displayed does not include any applicable pay practices (e.g., shift differentials, overtime, etc.). The pay range does not include the value of Cleveland Clinic's benefits package (e.g., healthcare, dental and vision benefits, retirement savings account contributions, etc.). Cleveland Clinic Health System is pleased to be an equal employment employer: Women / Minorities / Veterans / Individuals with Disabilities