Clinical Research Program Lead

The Clinical Research Program Lead (CRPL) will support clinical trials, studies, and implementation science research for a subspecialty clinic in the Heart Center. This position will provide direct support to the principal investigator(s), including developing program strategy. The CRPL will be responsible for overseeing all research activities in the clinic including IRB submission, regulatory oversight, participant enrollment, participant activity coordination, and data collection. They will also be responsible for managing project timelines and coordinating collaboration between divisions, centers, national and international partners. In addition, the CRPL will be responsible for coordinating grant proposals, study design, and CRF development. This will include drafting documents including federal and non-federal grant awards, protocols, and potentially manuscripts and abstracts. 

The position will interface with faculty, collaborators, and administration to report project progress and trouble shoot barriers. Outstanding communication and organizational skills, the ability to proactively manage challenges, and strong attention to detail are required. The individual is supervised by a Clinical Research Program Manager/Director and the Principal Investigator.

The earliest start date for this position is July 1, 2025. 

Minimum Education
B.A. BA/BS degree in science, technical, or health-related field with > 5 year relevant experience MS degree with 3 years relevant experience; Doctoral degree with > 2 years of relevant experience.

Minimum Work Experience
2-4 years of clinical research experience or an equivalent combination of relevant education and/or experience managing NIH or industry sponsored clinical research projects. Supervisory/management experience in related job function. 

Experience in one or several of the following fields is preferred: pediatrics, cardiology, prevention, rare disease, chronic disease, public health, sports science, or digital health. Strong scientific writing skills are required. 

Functional Accountabilities
Responsible Conduct of Research

• Consistently demonstrate adherence with the standards for the responsible conduct of research.

• Maintain confidentiality of data as required.

• Plan, conduct, and manage research and/or research intervention projects within the federal and institutional regulations and policies under the direction of the principal investigator.

• Responsible for appropriate use of research funds and resources.

• Comply with all annual job-related training requirements.

Communication

• Protect patient/family right to confidentiality in relation to research protocol.

• Act as a role model for other professionals by communicating responsively, respectfully, and assertively.

• Collaborate with physician and other health care professionals throughout all phases of the research process.

Project Management

• Effectively manage day-to-day research and/or research intervention program operations.

• Ensure that sponsor/data center deadlines are met.

• Ensure timely IRB submissions and adheres to all reporting requirements.

• Clearly and concisely documents patient assessments, observations, test results, and other study related information per federal regulations/ICH guidelines, GCPs, SOPs, sponsor/CRO and IRB requirements.

• Oversee subject recruitment and study enrollment goals. Determines effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials.

• Manage resources within study budget, works with senior staff and principal in