Research Support - Laboratory/Non-Laboratory, Staff/Administrative
Employment Type: Permanent Staff (SHRA)
Vacancy ID: P010519
Salary Range: $63,972 - $71,183
Lineberger Comprehensive Cancer Center’s Clinical Protocol Office is recruiting for 2 Nurse Consultant (Study Coordinator) positions. PLEASENOTE – WHENAPPLYINGFORTHISPOSITIONYOUWILL BE APPLYINGFORTHEFOLLOWINGTWOPOSITIONS: 20011691 & 20011692
The purpose of this position is to facilitate the conduct of oncology clinical trials, including subject and data management, according to federal regulations, Good Clinical Practice, and local and institutional policies. These responsibilities relate to the mission of the UNC/LCCC Protocol Office by maintaining the quality of research and by addressing patient safety and regulatory compliance which impact research quality and safeguard institutional integrity.
The primary responsibilities of this position include the informed consent process, eligibility and screening, toxicity assessment, patient management, conducting in-services for nurses staff in treating clinic; planning of patient recruitment methods; logistics of patient visits; logistics of obtaining and coordinating clinical samples; specimen collection as needed, enlistment of support of necessary ancillary departments; coordinating the ordering of the required supplies; preparation of study tubes, collecting source documentation; Data entry / management for assigned studies, working with Clinical Research Associates to facilitate data collection for CRFs (case report forms) and/or eCRFs for trials as assigned; prepare and participate in monitoring visits; facilitate pre-site meetings, site initiation meetings, and plan, organize and run protocol start-up meetings.
Education and Experience:
Licensed to practice as a Registered Nurse in the State of North Carolina and two years of experience in the area of specialization.
Knowledge of ICHGCP, Federal Regulations and Guidelines and ability to follow established regulations, procedures, and protocols; strong computer skills; ability to gather data and document procedures; ability to plan work and coordinate multiple projects; adequate social acumen and customer service skills; ability to communicate effectively and professionally verbally and in writing.
Ability to work on evenings, weekends and/or holidays occasionally required.
Previous experience with therapeutic clinical research involving drugs and/or devices. Experience in Phase I, II, and III clinical research. Experience navigating medical records and data extraction. SOCRA/ACRP Certification. One plus years of study coordinator experience or experience in oncology clinical trials and one plus year of oncology study coordinator experience.
The University of North Carolina at Chapel Hill is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to age, color, disability, gender, gender expression, gender identity, genetic information, race, national origin, religion, sex, sexual orientation, or status as a protected veteran.
Internal Number: 166655
About The University of North Carolina at Chapel Hill
Carolina rates among the nation’s great institutions of higher education, set on an historic and beautiful campus that celebrates all four seasons. Carolina’s students, faculty and staff come here from around the world, bringing varied cultural, racial and ethnic heritages that help make UNC-Chapel Hill a thriving intellectual center. We’re repeatedly ranked the nation’s best value in higher education for students seeking to earn a college degree – the University has garnered the top spot each time since the ranking’s launch in 1998.Whether you’ve just started your career, are new to academia or are a seasoned professional with assorted campus experiences to draw on, we hope you will find a great place at Carolina.