CLINICAL RESEARCH NURSE C

Location
Philadelphia, Philadelphia County
Posted
Apr 02, 2014
Employment Type
Full Time

Duties: Clinical Research Nurse B ; With minimal supervision, coordinate the conduct of Phase I - IV clinical trials including consenting, screening and enrolling eligible subjects, managing subject treatment per protocol, oversight and coordination of research testing, including labs, office visits and radiology exams, provide oversight for research medication administration, monitor patient care, treatment side effects and patient status throughout study period, communicate any research issues to PI and primary MD, communication with research team, including Investigators, CRC and regulatory team, to ensure patient safety and proper study conduct, provide patient/family education and support, follow GCP guidelines in the conduct of trials, coordinate implementation of research protocols with study and clinical team, collecting and reporting research data, reporting serious adverse events per protocol, coordinate subject care with clinical team, provide coverage and support to other research nurses and coordinators, maintain good communication with supervisors, co-workers and study team, attend study related meetings that may occur outside of usual work ours, other duties as assigned.

Clinical Research Nurse C: Independently coordinate the conduct of Phase I - IV clinical trials including consenting, screening and enrolling eligible subjects, managing subject treatment per protocol, oversight and coordination of research testing, including labs, office visits and radiology exams, provide oversight for research medication administration, monitor patient care, treatment side effects and patient status throughout study period, communicate any research issues to PI and primary MD, communication with research team, including Investigators, CRC and regulatory team, to ensure patient safety and proper study conduct, provide patient/family education and support, follow GCP guidelines in the conduct of trials, coordinate implementation of research protocols with study and clinical team, collecting and reporting research data, reporting serious adverse events per protocol, coordinate subject care with clinical team, provide coverage and support to other research nurses and coordinators, maintain good communication with supervisors, co-workers and study team, possibly assist in the writing and development of investigator-initiated protocols, participate in the development of unit SOP's, serve as a resource for junior staff, serve as a resource for development of study orders, provide input into the development of efficient work flows, attend study related meetings that may occur outside of usual work ours, other duties as assigned.

Qualifications: Clinical Research Nurse B: Registered Nurse with license to practice in the State of Pennsylvania and 1 year of nursing or clinical nursing experience required. BS degree in Nursing or a BA degree in a related discipline with oncology nursing experience or clinical research experience is highly preferred.
Must possess strong computer skills and working knowledge of Microsoft Office tools (e.g. Word, Excel, PowerPoint, etc.)

Clinical Research Nurse C: The same as above with a minimum of 2 to 3 years of nursing or clinical research experience required.

Position contingent upon funding.

Reference Number: 40-17156

Salary Grade: 027

Employment Type: Exempt

Org: CC-Cancer Center

Special Requirements: Background Check Required

Job Family: J-Technical/Professional Medicine/Health