Job Seeker Home
(this posting is closed/inactive)
Oncology Clinical Research Coordinator - Oncology Administration
Greenwich, CT 06830 United States
At Greenwich Hospital, a 206-bed regional provider of care and affiliate of Yale New Haven Health, you'll find a hospital and a working culture like no other. Conveniently located minutes from I-95, I-684, I-287, the Merritt/Hutchinson Parkway and Westchester County - and close to public transportation and shuttle service - Greenwich Hospital offers a beautiful state-of-the-art facility that serves as a national model for advanced health care design. Our unwavering commitment to care has been recognized by the Press Ganey Summit Award for four consecutive years of patient satisfaction scores above the 95th percentile... and extends to building extraordinary careers.
This person must be able to meet our 7 Standards for Exceptional Service which include: treat people we serve as guests; respect people's privacy & confidentiality; present a professional image; answer the telephone professionally; listen first, then act promptly; anticipate people's needs, then act to provide it; and maintain a safe & clean environment. If you have a passion to exceed customer's expectations and want to provide excellent clinical service, you have found the right team!
Oversee & facilitate clinical research studies with MDs.
Assist MD in obtaining Institutional Review Board approvals of trials; Serious Adverse Event Reports.
Assist Program Director of Oncology with contracts/budgets associated with clinical trials.
Identify patients who might be eligible for clinical trials; work w/MD in applying inclusion/exclusion criteria.
Promote clinical trials at GH by keeping MDs & other staff advised of current trials.
Educate staff (RNs, pharmacy, lab, radiology) re: clinical research process.
Coordinate care for patients on clinical trials (MD appt., Rx schedule, pharmacy, lab, radiology, RT).
Teach/instruct patient/family re: the clinical trial & their Rx; assist w/informed consent process.
Act as liasion to sponsors of trials (both pharmaceutical & cooperative studies); liaison for prestudy, initiation & ongoing monitoring visits.
Data input (both written & computer); Complete case report forms & answer queries w/MD from sponsors.
Knowledge of current nursing/medical practice in Oncology; Strong written & verbal communication skills; Ability to coordinate & oversee adherence to clinical trial protocols; Detail-oriented with good organization skills. Must have Oncology experience. Critical thinking, work independently, computer proficiency are musts. Must be familiar with contracts and budgets associated with trials.
CT licensed RN, in good standing. Must have BSN and OCN certification. Minimum 5 years of nursing experience.
Part-time 3 days per week. This position will be full-time in Spring/Summer 2013.
HR Use Only: hjgp Job Number: 38085
Education, training, experience:
Terms & Conditions