Clinical Research Nurse D

University of Pennsylvania•Philadelphia, PA

4d•Onsite

About The Position

Provides leadership in the coordination of clinical trials and unit-related projects. Oversees study approvals, participant enrollment and consent, visit scheduling, medication administration, data collection, and regulatory documentation to ensure compliance with institutional and sponsor requirements. Serves in a lead capacity by guiding research coordinators and assistants, supporting project timelines, and preparing for monitoring visits and audits.

Requirements

Bachelor's degree and 5-7 years of experience
Registered Nurse with Licensure in Commonwealth of Pennsylvania without restriction or limitation required.

Nice To Haves

BSN preferred.

Responsibilities

Ensure proper screening and enrollment of all study participants, including administering informed consent and confirming subject study eligibility prior to participation
Ensure proper reporting of serious and non-serious adverse events to the Sponsor and all applicable institutional or study related committees and personnel according to applicable regulations and policies
Coordinate the administration of the investigational product and study related medications including obtaining orders, scheduling administration dates, administration of investigational and study related medications (as applicable), monitoring subjects for post-administration adverse events or reactions
Meet with Principal Investigator routinely to discuss study related issues and to ensure completion of study related procedures.
Ensure preparation of all required study related documents for submission to all applicable institutional committees for review and approval to start trial.
Ensure preparation of study related document templates (e.g., visit guides, source document templates), subject study binders, regulatory binders (hard and electronic version), patient list (enrollment log) for study start up
Manage scheduling and coordination of subject study specified treatment, follow-up visits and procedures.
Manage collection of data from source documents pertaining to study visits and transcribe to case report form, including concomitant medications and adverse events
Assist with protocol development to ensure logistical feasibility of all study related procedures and study work-flow
Orient and mentor new unit staff and function as resource for current staff
Other duties and responsibilities as assigned

Benefits

comprehensive medical, prescription, behavioral health, dental, vision, and life insurance benefits
flexible spending accounts to pay for eligible health care and dependent care expenses with pre-tax dollars
exceptional tuition benefits for employee, spouse, and dependent children
tuition assistance at other institutions for dependent children
generous retirement plans (Basic, Matching, and Supplemental)
pre-tax or Roth basis retirement savings
wide variety of investment options through TIAA and Vanguard
substantial amount of time away from work
long-term care insurance
wide variety of programs and resources to help care for health, family, and work-life balance
array of resources to help advance personally and professionally
access to a wide range of University resources as well as cultural and recreational activities
free or discounted admission and memberships to arts and cultural centers and museums
substantial savings on other goods and services such as new cars from Ford and General Motors, cellular phone service plans, movie tickets, and admission to theme parks
flexible work options offer creative approaches for completing work while promoting balance between work and personal commitments
forgivable loan for eligible employees interested in buying a home or currently residing in West Philadelphia
reimbursement for qualified expenses in connection with the legal adoption of an eligible child