Clinical Research Nurse - Home Visits (PRN); Tulsa, Oklahoma

WEP Clinical•Tulsa, OK

22d•Onsite

About The Position

The Clinical Research Nurse provides nursing care to clinical trial participants in their homes and supports study procedures and protocol compliance. The work is project-based and PRN/per diem, with no guarantee of hours or assignments. Project timelines and visit frequency depend on study needs and geographic location. The nurse typically drives up to 1–2 hours to visit patients and uses their own vehicle. Study-specific orientation and materials are provided. Compensation covers onsite visit time at $55 per hour and travel time at $50 per hour, with mileage reimbursement per project or contract terms. The role requires independent work, attention to detail, patient-safety focus, and protection of data integrity. The nurse performs study-related procedures, educates participants, documents visit activities, and communicates findings and concerns to study teams. WEP Clinical describes its work as partnering with biopharmaceutical sponsors to deliver clinical trials, home health services, expanded access programs, and market access consultancy. The company reports more than 15 years of global experience and programs across 150+ countries.

Requirements

Active, unrestricted nursing licensure.
Graduate of an accredited BSN, Associate Degree in Nursing, or Nursing Diploma program.
At least 2 years of post-qualification acute care experience.
BLS certification.
Basic IT proficiency, including mobile devices, documentation systems, and Microsoft tools.
Ability to work independently in home-based settings.
Valid driver's license and reliable transportation.
Training in handling and transporting hazardous substances, or willingness to receive training.
Flexible schedule.

Nice To Haves

Clinical research experience preferred.
ICH-GCP certificate, or willingness to obtain one.

Responsibilities

Provide high-quality nursing care to clinical trial participants in their homes.
Perform study procedures, including vital signs, specimen collection, processing and shipment, and electrocardiograms (ECGs).
Administer investigational medications or products according to study protocol.
Assess patients, monitor for adverse events, and report findings to the study team or Principal Investigator.
Document visit activities accurately in accordance with study requirements.
Educate patients about study procedures, medications, and compliance.
Adhere to ICH-GCP guidelines and study protocols.
Communicate effectively with patients, caregivers, and study teams.
Protect patient privacy and securely handle confidential protected health information in accordance with HIPAA and applicable regulations.
Advocate for patients, participants, and their families.
Work autonomously, recognize limitations, and escalate concerns appropriately.
Follow ethical research requirements, including protections for vulnerable populations.