Clinical Research Coordinator-Sweitzer (Durham, NC, US, 27710)

School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate translation of fundamental scientific discoveries to improve human health locally and around the globe. Composed of more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more than 6,200 staff, the Duke University School of Medicine along with the Duke University School of Nursing, and Duke University Health System comprise Duke Health, a world-class academic medical center. The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Health Integrated Practice, Duke Primary Care, Duke Home Care and Hospice, Duke Health and Wellness, and multiple affiliations.

CLINICAL RESEARCH COORDINATOR – Psychiatry – BEHAVIORAL MEDICINE AND NEUROSCIENCES DIVISION – SWEITZER

Be You.

Participates in or leads day to day operations of clinical research studies conducted by the Sweitzer Lab in the Department of Psychiatry and Behavioral Sciences at Duke North Pavilion; performs a variety of duties involved in the collection, compilation, documentation, and analysis of clinical research data. May oversee the work of junior staff and train or mentor others in clinical research tasks.

Our team is seeking a highly motivated candidate with excellent attention to detail, strong interpersonal skills, and willingness to learn. The CRC will provide support on multiple studies within the Sweitzer lab encompassing a diverse participant population, including people in recovery from Opioid Use Disorder, people who smoke, and people with chronic pain. As a CRC working in this lab, you will be responsible for regulatory and administrative tasks, as well as proper documentation and study procedures for participants starting at screening and through study completion. Some study procedures that you will be responsible for are: recruitment, screening, participant scheduling and communication, consenting, inventory and accountability of investigational product, assisting with fMRI sessions, administering surveys and questionnaires, documenting adverse events, maintaining enrollment logs, maintaining and ordering equipment, and developing and submitting documentation for Institutional Review Board (IRB) review.

A flexible schedule is required, including assisting with occasional evening and weekend study visits.

Minimum Requirements:

• Work requires completion of an associate’s degree
• Work requires a minimum of two years of relevant research experience. A Bachelor’s degree may substitute for 2 years required experience

Preferred Qualifications:

• Minimum one year of clinical research experience
• Experience or interest in working with addiction populations
• Experience working in REDCap
• Familiar with Duke systems and processes

Other Requirements:

• This is a fully onsite position with occasional remote work opportunities
• Some evening and weekend flexibility is required to accommodate participant scheduling needs

Be Bold.

Position Description:

• Participates in or lead day-to-day operations of clinical research studies
• Employs and may develop strategies to maintain recruitment and retention rates and evaluate processes to identify problems. Escalates issues.
• Screens participants for complex studies. Develops or helps develop SOPs.
• Conducts activities for study visits in compliance with the protocol.
• Identifies adverse events (AEs), and determines whether or not they are reportable. Collaborates with the PI to determine AE attributes, including relatedness to study.
• Enters and collects data, and develops data entry or collection SOPs or tools.

• Ensures that studies are conducted in compliance with institutional requirements and other policies

• Knowledgeable in regulatory and institutional policies and processes; applies knowledge appropriately in study documentation, protocol submissions, and standard operating procedures (SOPs).
• Develops and submits documentation for Institutional Review Board (IRB) review in iRIS. Communicates with the IRB staff and reviewers, and handles issues appropriately.

Choose Duke.

The Department of Psychiatry & Behavioral Sciences, founded in 1943, is one of 26 departments in the Duke University School of Medicine (SOM). The department is comprised of more than 500 faculty, staff, and trainees. Our goal is to help people with behavioral health challenges live their best life. We pursue this goal through a three-fold mission of superior specialty and integrated patient care for all, ground-breaking research, and exceptional training and education.

Duke University is consistently ranked among the top universities worldwide and is renowned for its cutting-edge research across disciplines. Beyond the engaging work, you'll also benefit from Duke's competitive benefits package, including health insurance plans, generous paid time off, retirement programs with employer contributions, tuition assistance for employees and their children, and more.

Screening of Applications:

• Screening continues until position is filled. [Hiring team must screen applications as they come in and must continue screening ALL applications until position is filled.]