"Clinical Research Coordinator A (Department of Obstetrics and Gynecology)"

This position will assist in the management of an NIH-funded investigator-initiated clinical trial with responsibilities in the Division of UroGynecology. The incumbent will coordinate: the screening of patients, subject enrollment, and collection of clinical data at study visits. Additionally, the incumbent may assist with Institutional Review Board (IRB) filings and inquiries, the preparation of manuscripts, grant proposals, and research related presentations. They will work closely with the Principal Investigator, Director of Research Operations, and study team to identify problems and develop solutions. They will be expected to implement approved changes to procedures as needed and monitor results. Finally, they may also be responsible for providing study coordination for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects as needed.

This position will support the Division of UroGynecology, which conducts clinical research on topics involving pelvic floor health including urinary and fecal incontinence, and prolapse surgeries. This research program is fully integrated within the Urogynecology clinics and researchers will work closely with clinical staff and patients. Our goal is to improve pelvic floor health and lives of all people. We seek applicants who connect with this clinical mission.

The primary responsibilities of this position are:

• Study recruitment: Interview and evaluate participants as potential candidates for enrollment into clinical trials. Obtain informed consent and conduct enrollment visits at multiple study sites by telephone and at subject’s homes.
• Study visit scheduling and follow-up. Plan, direct, and assess overall study management of participants. Intercept and respond to trial participant phone calls. Perform telephone and in-person follow-up as per study protocol.
• Participate in the review and preparation of protocols for original, pharmaceutical, and government clinical trials. Prepare protocols, informed consent, data collection forms and advertisement for regulatory approval.
• Organize and participate in site visits from the study sponsor and regulatory authorities. Attend investigator meetings for clinical research trials as needed.

Qualifications: Bachelor's Degree with 1-2 years of related experience in research and clinical study methodologies or equivalent combination of education and experience is required. Applicants must be well-organized and able to flexibly manage diverse responsibilities. Applicant must work well as part of a team. Comfortable with computers/technology, especially basic programs such as MS Word, Excel, etc. Fluency in Spanish is preferred. Preferred that applicant have a driver’s license and vehicle. A strong interest in women's health is warmly encouraged and must enjoy working with senior women. Position requires a highly motivated, friendly, and articulate individual with excellent verbal and written communication skills. The candidate should possess the ability to work independently and also as part of a team. Strong planning, organizational and prioritizing capabilities along with problem solving skills desired. Must be willing to work some flexible hours when needed (occasional evening coverage, primarily). This position is contingent upon grant funding.