Academic ConnectClinical Research Nurse C (OBGYN - GYN Oncology)
Job Description Summary
This role supports the GYN Oncology Division within the Department of Obstetrics & Gynecology. Independently coordinate, with the support of the study team, state of the art clinical trials, including consenting, screening and enrolling eligible subjects, managing the treatment of patients throughout their participation in the study including education about any adverse effects they might experience, provide oversight and coordination of research testing and follow-up, as well as, in some case, directly administer novel research medications. Monitor the care and progress of patients, the treatment of any side effects and status of patients throughout their participation in the study, in addition to providing patient/family education and support. May assist in the writing and development of investigator-initiated protocols, participate in study specific EPIC Beacon build, develop SOPs, educate and train clinical and research staff, serve as a resource for junior staff. Provide input into the development of efficient work flows and attend any meetings related to the studies. Develop and institute internal strategies for meeting and exceeding trial enrollment, and assure compliance with all relevant regulatory standards. Help develop internal budgets for sponsored trials and assist in the development of investigator-initiated trials.
Job Responsibilities
- Coordinate clinical trials, including consenting, screening and enrolling eligible subjects, managing patient treatment throughout participation in the study including education about any adverse effects they might experience,
- Provide oversight and coordinate research testing and follow-up, as well as, in some case, directly administer novel research medications.
- Monitor care and progress of patients and any side effects; provide patient/family education and support.
- Assist in writing investigator-initiated protocols, participate in study specific EPIC Beacon build, develop SOPs,
- Educate and train clinical and research staff, serve as a resource for junior staff.
- Provide input into the development of efficient work flows and attend study meetings.
- Develop and institute strategies for meeting and exceeding trial enrollment, and assure compliance with all relevant regulatory standards.
- Help develop internal budgets for sponsored trials and assist in the development of investigator-initiated trials.
- Other duties and responsibilities as assigned
Position Contingent upon funding
Qualifications
- Registered Nurse with a current PA license without restriction or limitation and 2-3 years of experience required. BSN degree preferred. Position requires an individual with excellent oral 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 able to work flexible hours. Previous research experience and knowledge of IRB processes, human research protection regulations, and regulatory management preferred. Background in oncology preferred.
Job Location - City, State
Philadelphia, Pennsylvania
Department / School
Perelman School of Medicine
Pay Range
$62,000.00 - $79,421.00 Annual Rate
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