Clinical Research Project Manager

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Job Title

Clinical Research Project Manager - DDI

Location

Weston

Facility

Krupa Center Weston

Department

Research Administration-Research Innov and Educ

Job Code

T26213

Shift

Days

Schedule

8:30am-4:30pm

Job Summary

Job Details

Join the Cleveland Clinic Florida team at the Krupa Center in Weston, where you will work alongside highly skilled and compassionate caregivers and board-certified family practice physicians to provide patient-first healthcare. Cleveland Clinic is consistently recognized as one of the top hospitals in the nation, offering quality preventive care, management of chronic conditions and comprehensive services for the entire family. At Cleveland Clinic, you will receive strong support and recognition, collaborate with dedicated professionals and build a rewarding career with one of the world’s most respected healthcare organizations.  

As a Clinical Research Project Manager for the DDI team, you will oversee the administrative functions of single- and multi-institutional research trials while managing the daily operations and organizational activities of Phase I–IV clinical studies. This role combines both patient-facing and administrative responsibilities, with approximately 60% of time spent directly interacting with patients and 40% focused on study coordination and management activities. You will coordinate IRB submissions, collect research data from participants, draft study protocols, and facilitate communication among investigators, patients, and international collaborators.

The research program is dedicated to improving quality of life following cancer surgery, placing patients at the center of every project. Working closely with patient partners, you will help incorporate their perspectives into research design and execution, fostering a collaborative approach that enhances the patient’s experience and advances meaningful, patient-centered outcomes.

A caregiver in this role works days from 8:30 a.m. – 4:30 p.m.

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) as required by the Responsible Conduct of Research guidelines adopted by the Cleveland Clinic.

• Perform other duties as assigned.

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 

• Background/ability or working with clinical studies and clinical research team members at all levels

• Within 90 days of hire, must successfully complete training in Human Subjects Research (HSR) as required by the Responsible Conduct of Research guidelines adopted by the Cleveland Clinic

Preferred qualifications for the ideal future caregiver include:  

• Master’s degree

• Society of Clinical Research Associates (SOCRA) or Association of Clinical Research Professionals (ACRP) Certification

• Investigator-initiated research experience 

• Experience with grant or budget management for investigator-held studies 

• Five years of research experience

• Supervisory experience 

• Experience working with contracts or agreements

• Experience with NIH or other government body funding

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.

The policy of Cleveland Clinic Health System and its system hospitals (Cleveland Clinic Health System) is to provide equal opportunity to all of our caregivers and applicants for employment in our drug free environment. All offers of employment are followed by testing for controlled substances.

Cleveland Clinic Health System administers an influenza prevention program. You will be required to comply with this program, which will include obtaining an influenza vaccination on an annual basis or obtaining an approved exemption.

Decisions concerning employment, transfers and promotions are made upon the basis of the best qualified candidate without regard to color, race, religion, national origin, age, sex, sexual orientation, marital status, ancestry, status as a disabled or Vietnam era veteran or any other characteristic protected by law. Information provided on this application may be shared with any Cleveland Clinic Health System facility. 

If applying for a Florida position, please see the following website for more information on the background screening requirements required by the Agency of Health Care Administration: https://info.flclearinghouse.com/

Please review the Equal Employment Opportunity poster. 

Cleveland Clinic is pleased to be an equal employment opportunity employer.