Clinical Research Coordinator A (OBGYN - PEACE Family Planning)

Requirements

• Bachelor's Degree with 1-3 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/tech

Benefits

Additional Information

University Overview The University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned leader in education, research, and innovation. This historic, Ivy League school consistently ranks among the top 10 universities in the annual U.S. News & World Report survey. Penn has 12 highly-regarded schools that provide opportunities for undergraduate, graduate and continuing education, all influenced by Penn's distinctive interdisciplinary approach to scholarship and learning. As an employer Penn has been ranked nationally on many occasions with the most recent award from Forbes who named Penn one of America's Best Large Employers in 2023. Penn offers a unique working environment within the city of Philadelphia. The University is situated on a beautiful urban campus, with easy access to a range of educational, cultural, and recreational activities. With its historical significance and landmarks, lively cultural offerings, and wide variety of atmospheres, Philadelphia is the perfect place to call home for work and play. The University offers a competitive benefits package that includes excellent healthcare and tuition benefits for employees and their families, generous retirement benefits, a wide variety of professional development opportunities, supportive work and family benefits, a wealth of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator A (OBGYN - PEACE Family Planning) Job Profile Title Clinical Research Coordinator A Job Description Summary This position will assist in the management of multiple clinical trials and responsibilities in the Division of Family Planning. The incumbent will coordinate: the screening of patients, subject enrollment, collection and storage of biological samples and related study documents, and collection of clinical data. 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 will be responsible for study coordination for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects. Job Description Job Responsibilities This position will support the Division of Family Planning , which conducts clinical research on topics such as contraception, abortion, and miscarriage. This research program is fully integrated within the Family Planning clinic and researchers will work closely with clinical staff and patients. Our goal is to improve the reproductive 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 (e.g., 3737 Market Street, Pennsylvania Hospital, Philadelphia Women's Center) Study visit scheduling and follow-up: provide clinical services, including phlebotomy and processing biospecimens. Plan, direct, and assess overall study management of participants. Intercept and respond to trial participant phone calls. Perform telephone 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. Other duties and responsibilities as assigned Our research staff includes 4-5 research coordinators and a Director of Research Operations. We use a team approach to coordinating research studies, and our coordinators will be able to work on a variety of projects as both a primary and backup coordinator. Our team is a mix of long-term and shorter-term research coordinators, and we welcome applicants on a healthcare profession track seeking to gain research experience. The incumbent may work in multiple locations within Philadelphia, including Penn Medicine University City, HUP, Penn Presbyterian, and off-site clinics such as the Philadelphia Women's Center. *Position contingent upon continued funding*

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