Clinical Research Nurse D
University of Pennsylvania Perelman School of Medicine•Philadelphia, PA
•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
- excellent healthcare
- tuition benefits for employees and their families
- generous retirement benefits
- a wide variety of professional development opportunities
- supportive work and family benefits
- a wealth of health and wellness programs and resources
- 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
- tuition assistance for employee, spouse, and dependent children
- generous retirement plans
- substantial amount of time away from work
- long-term care insurance
- wellness and work-life resources
- professional and personal development resources
- access to a wide range of University resources as well as cultural and recreational activities
- discounts and special services
- flexible work options
- forgivable loan for eligible employees interested in buying a home or currently residing in West Philadelphia
- adoption assistance
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
