Clinical Research Professional/Senior Clinical Research Prof, Internal Medicine, Pulmonary Division

This person will contribute to groundbreaking research that addresses the health impacts of climate change and rising temperatures and develop expertise in the use of wearable sensors and transcriptomic analysis in a public health context. This person will be a part of adedicated research team that values collaboration and innovation, opportunities for professional growth and development in a supportive environment.

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 faculty are transforming the world of medicine every day. The Department of Internal Medicine is a top-tier department with world-renowned faculty and staff.

A full time clinical research professional position is available in the Department of Internal Medicine, Division of Pulmonary, Critical Care and Sleep Medicine at the University of Cincinnati College of Medicine.

We are seeking an experienced and detail-oriented Clinical Research Professional or Sr Clinical Research Professional to join our research team. The final staff title (CRP or Sr CRP) will be commensurate with the candidate's experience and qualifications. This position will support a clinical research project focused on understanding the impact of extreme heat exposure on heat-related illness (HRI) and immune response in vulnerable populations, including firefighters and elderly residents. This role is integral to the success of a study addressing the health risks posed by climate change and extreme temperatures, contributing to the development of personalized strategies for HRI risk management. This position is expected to be a hybrid position.

• Coordinate and oversee day-to-day research activities, ensuring all aspects of the project are executed smoothly and on schedule.
• Lead recruitment efforts for study participants, including firefighters participating in live burn training and elderly individuals from neighborhoods at risk for extreme heat exposure.
• Manage participant visits, including the collection of biometric data (e.g., core body temperature, heart rate, heart rate variability), administration of surveys, and collection of nasal swab and blood samples.
• Maintain accurate and organized records of study data, ensuring adherence to research protocols, IRB requirements, and data privacy standards.
• Coordinate with community organizations and external stakeholders to facilitate participant recruitment and data collection efforts.
• Manage data entry, quality control, and preliminary analysis, including biometric data from wearable devices and sensors.
• Prepare and update study-related documentation, such as informed consent forms, protocols, and IRB submissions.
• Work closely with UC and UC Health offices in negotiation of contracts, confidentiality agreements and amendments related to the conduct of research activities.
• Assist in the management of samples for RNA sequencing and bioinformatics analysis.
• Serve as a key point of contact for study participants, research team members, and external partners to ensure clear communication and project progress.
• Perform related duties based on departmental need. This job description can be changed at any time.

Clinical Research Professional:

Required Education

• Bachelor's degree in public health, biology, nursing, or a related field.
• Five (5) years of relevant work experience and/or other specialized training can be used in lieu of education requirement.

Required Experience

One (1) year of experience in research coordinator in clinical or community-based studies.

- OR -

Senior Clinical Research Professional:

Required Education

• Bachelor's degree in public health, biology, nursing, or a related field.
• Seven (7) years of relevant work experience and/or other specialized training can be used in lieu of education requirement.

Required Experience

Three (3) years of experience in research coordination in clinical or community-based studies.

• Master's degree.
• Strong organizational and project management skills with the ability to manage multiple tasks and priorities.
• Excellent communication and interpersonal skills, with demonstrated experience in participant recruitment and engagement.
• Proficiency in data management software (e.g., REDCap, Excel) and familiarity with wearable technology data.
• Experience in collecting biological samples (e.g., nasal swabs, blood) is ideal, with training available as needed.
• Ability to work independently and collaboratively in a dynamic research environment.
• Strong commitment to data confidentiality and ethical research practices.