Clinical Research Project Manager, College of Medicine, Department of Neuro at University of Cincinnati

Cincinnati, Ohio, United States -

Full Time

Start Date

Immediate

Expiry Date

20 Dec, 25

Salary

0.0

Posted On

21 Sep, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Project Management, Communication Skills, Problem-Solving, Organizational Skills, Leadership Skills, Attention to Detail, Teamwork, Self-Discipline, Motivation, Regulatory Compliance, Clinical Study Procedures, Clinical Documentation, Training Development, Budget Management, Timeline Management

Industry

Higher Education

Description

Current UC employees must apply internally via SuccessFactors Next Lives at the University of Cincinnati Founded in 1819, the University of Cincinnati ranks among the nation’s best urban public research universities. Home to more than 53,000 students, 12,000 faculty and staff, and over 350,000 living alumni, UC, a Carnegie 1 institution, combines research prowess with a physical setting The New York Times has called “the most ambitious campus design program in the country." UC's momentum has never been stronger as the anchor of the Cincinnati Innovation District, the oldest cooperative education (co-op) program in the country with students earning $88.8 million annually through paid experiences, an academic health system, and as a member of the Big 12 Conference. The university contributes $10.6 billion in economic impact to the city and $22.7 billion to the state of Ohio. At UC, next is all of us. Learn more at uc.edu. UC is a mission-driven organization where we are committed to student success and positively transforming the community through scholarship and service. We thrive on innovation, making an impact, and fostering an environment where staff and faculty are key contributors to UC’s success. Job Overview As one of the oldest medical schools in the country, the University of Cincinnati College of Medicine (COM) has a reputation for training best-in-class health care professionals and developing cutting-edge procedures and research that improves the health and clinical care of patients. In partnership with the UC Health academic healthcare system and Cincinnati Children’s Hospital Medical Center, College of Medicine’s doctors and faculty are transforming the world of medicine every day. The Department of Neurology & Rehabilitation Medicine is a top-tier department with world-renowned faculty and staff. With world-class research, teaching and medical practice opportunities, why not choose the University of Cincinnati College of Medicine? UC is one of the largest employers in the Cincinnati region, employing over 15,000 full-time and part-time faculty, staff and student workers. Founded in 1947, the UC Department of Neurology and Rehabilitation Medicine is revolutionizing medicine by connecting discovery and education to world-class care in neurological diseases. Our vision is to be the model organization that integrates neurologic clinical care, research and education. The University of Cincinnati, College of Medicine, Department of Neurology and Rehabilitation Medicine is seeking a full-time Clinical Research Project Manager for the NIH-funded StrokeNet Thrombectomy Endovascular Platform (STEP) clinical trial. STEP is a unique, first-of-its-kind platform trial that is looking at various treatments for patients with an Acute Stroke. As the Prime Project Manager of, the candidate will oversee several aspects of national project management for this unique clinical trial. The project manager will work directly with performance sites in the clinical trial. The appropriate candidate should have a clinical background and extensive clinical research experience.Essential Functions Monitor and report on the progress of delegated clinical trials, which includes budgets and timelines. Prepare, oversee, and review documents that are related to the assigned clinical study. Arrange or help in organizing clinical study meetings. Ensure the availability of necessary resources for the execution of clinical projects. Help develop training materials and train clinical staff at sites. Communicate with sites regarding key study updates during study webinars and other avenues. Lead the clinical project team and various study team meetings. Fully involved in resolving issues; take part in procedure improvement initiatives. Attain clinical study goals by working with other members of the study team to outline their priorities, and to also resolve conflicts that may come up in the project process. Work hand-in-hand with the study team to manage documents that are related to the clinical study. Responsible for maintaining the protocol versions and manual of procedures for the trial. Help prepare safety reports in collaboration with clinical leaders of the project and sites. Work collaboratively with team members to ensure regulatory compliance. Perform related duties based on departmental need. This job description can be changed at any time. Required Education Bachelor’s Degree. Nine (9) years of relevant work experience and/or other specialized training can be used in lieu of education requirement. Required Experience Five (5) years related experience.Additional Qualifications Considered Possess excellent communication skills so as to be able to effectively convey messages across to both study team members and other external people like vendors and external consultants. Good problem-solving, organizational, and leadership skills are highly required. Ability to work with little or no supervision. Ability to pay keen attention to detail at all times. Must be able to work within stipulated timeframes or deadlines even in the face of multiple responsibilities or projects. Must be able to work as part of a team or in most cases lead a team. Must have a ‘one of a kind’ work ethic, and must exhibit a great level of self-discipline. Ability to organize and motivate other members of the study team. Proficient user of basic computer applications for the execution of daily project operations. Experience in writing clinical study procedures and other clinical documents is a plus. Experience in an academic or clinical setting in the area of clinical specialization. SoCRA and/or ACRP certification. Physical Requirements/Work Environment Sitting - Continuously Compensation and Benefits UC offers an exceptional benefits package designed to support your well-being, financial security, and work-life balance. (UC Benefits Link) Highlights include: Comprehensive Tuition Remission UC provides tuition remission for you and your eligible dependents, covering tuition costs for nearly all undergraduate and graduate programs offered by the university. Robust Retirement Plans As a UC employee, you won’t contribute to Social Security (except Medicare). Instead, you’ll choose between state pension plans (OPERS, STRS) or an Alternative Retirement Plan (ARP), with UC contributing 14–18% of your salary based on position. Real Work-Life Balance UC prioritizes work-life balance with a generous time-off policy, including: Vacation and sick time 11 paid holidays and additional end-of-year paid time off (Winter Season Days) 6 weeks of paid parental leave for new parents Additional Benefits Include: Competitive salary based on experience Comprehensive health coverage (medical, dental, vision, prescription) Flexible spending accounts & wellness programs Professional development & mentorship opportunities To learn more about why UC is a great place to work, please visit our careers page at https://www.uc.edu/careers.html UC is an E-Verify employer. If hired into this position, you will be required to provide satisfactory proof of employment eligibility by providing acceptable, original forms of identification for employment verification via the Federal I-9 employment verification process. A list of acceptable documents can be seen here: https://www.uscis.gov/i-9-central/form-i-9-acceptable-documents Important: To apply you must create a profile and submit a complete job application through the UC applicant portal. We are unable to consider “easy apply” applications submitted via other websites. For questions about the UC recruiting process or to request accommodations with the application, please contact Human Resources at jobs@uc.edu. Equal Opportunity Employer. Building a workplace where all qualified applicants will receive consideration for employment, including Individuals with Disabilities and Protected Veterans. REQ: 99795 SF:OMJ SF:RM SF:HEJ, SF:INS SF:HERC SF:DIV SF:LJN SF:IHE

Responsibilities

The Clinical Research Project Manager will oversee various aspects of national project management for the NIH-funded STEP clinical trial, including monitoring progress, preparing documents, and leading study team meetings. The role involves direct communication with performance sites and ensuring regulatory compliance.