Description
Position Summary
At Stony Brook Medicine, a Study Coordinator is a valuable member of our team, who provides administrative support and has the ability to interface with all levels of management throughout the hospital.
Qualified candidates will demonstrate superior patient care and possess outstanding communication skills while adhering to our high standard of excellence.
Duties of a Study Coordinator may include the following but are not limited to:
- Recruit and enroll research subjects and schedule patients. Attend Tumor Board conferences, participate in hospital rounds and staff meetings and review surgical and pathology reports of cancer patients for potential candidates. Review patients on research therapies to assure toxicity and response to treatment. Follow and maintain records on protocol patients for the duration of the study.
- Coordinate multiple Oncology Cancer Clinical Trials from inception to closure under the direction of Principal Investigator/Cancer Clinical Trials Administrative Director. Includes screening, eligibility, data collection, adverse event reporting, completion of CRF's and all regulatory requirements per protocol.
- Plan and coordinate industry-sponsored, cooperative group and investigator initiated clinical research projects including meeting with industry representatives, contract coordination and budget negotiation. Acts as a resource between outside sponsors, industries and SUNY.
- Conducts informed consent process and discusses studies with patients.
- Patient/Staff Education - Educate patients and families as well as oncology staff on the research process and investigational cancer drugs.
- All other duties as assigned.
Qualifications
Required Qualifications: Bachelor's degree and at least 3 years of related full time experience in a clinical/healthcare setting to include working on clinical trials with proficiency in screening and enrolling research subjects, data collection, and adverse event reporting or, in lieu of degree, a combination of directly related education and experience totaling at least four years. Knowledge of medical terminology. Proficiency with Microsoft Word, Excel and PowerPoint. Excellent communication and organizational skills. Ability to work independently with minimal supervision.
Preferred Qualifications: Experience with coordinating multiple clinical trials, preferably in Oncology, and an understanding of the IRB/regulatory process. IRB training experience.
Special Notes: Resume/CV and cover letter should be included with the online application.
Posting Overview: This position will remain posted until filled or for a maximum of 90 days. An initial review of all applicants will occur two weeks from the posting date. Candidates are advised on the application that for full consideration, applications must be received before the initial review date (which is within two weeks of the posting date).
If within the initial review no candidate was selected to fill the position posted, additional applications will be considered for the posted position; however, the posting will close once a finalist is identified, and at minimal, two we
Compensation Information:
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