Enrollment Research Nurse

Join an industry leader in providing professional care as part of our nursing team. At McKesson, you’ll work in a more personalized environment, giving every patient the one-on-one time they need within each session. Whether this is your first role in nursing, or you have a history in healthcare, our extensive training will provide you with the skills you need to give patients the care they need while shaping the future of health.

• Facilitates patient enrollment in clinical trials by conducting recruitment, screening, enrollment, and follow-up activities in accordance with protocol requirements.
• Reviews the medical records of prospective study participants to confirm eligibility as defined by the protocol.
• Documents and evaluates medical history, concomitant medications, prior therapies, and adverse events.
• Utilizes the study protocol as the primary reference for patient screening.
• Informs and educates patients throughout the enrollment process, including screening and treatment steps.
• Provides the patient with information about available support services, including transportation, accommodation, and financial assistance.
• Reviews study design and inclusion/exclusion criteria with both physician and patient.
• Implements study-specific communications internally and externally as necessary.
• Verifies that all medications are approved by the protocol before starting treatment or when adjusting medication regimens, such as during crossover studies.
• Calculates and documents BSA, creatinine clearance, urine protein: creatinine ratio, or other protocol-required conversions accurately.
• Performs protocol-required screening assessments as applicable.
• Resolves clinical issues collaboratively with research staff as they occur.
• Completes and documents screening and eligibility procedures accurately.
• Develops study-specific tools for source documentation if not provided by the sponsor.
• Documents instances where patients are not eligible for a protocol and informs the physician accordingly.
• Ensures accurate and complete documentation of protocol requirements in line with site Work Instructions/SOPs.
• Shares site screening statuses through a weekly activity report with relevant site and management personnel.
• Communicates all protocol-related screening concerns to appropriate study colleagues.
• Verifies informed consent procedures and adheres to protocol requirements to protect study participants.
• Requests medical records of potential study subjects for eligibility review.
• Attends regular site research meetings.
• Participates in study-specific on-site meetings/visits, conference calls, and other coordinator meetings as required.

• Associate of Nursing Degree; Bachelor of Nursing is preferred.
• Nursing license for the State of Texas.
• Proficiency in HIPAA compliance, Good Clinical Practice (GCP), and FDA regulations.
• In-depth understanding of clinical research methodologies.
• One year of clinical nursing experience.
• One year of clinical research experience is preferred.
• One year of experience treating oncology patients is preferred.

• Medical, Dental, and Vision
• Health Spending Accounts
• Flexible Spending Accounts
• 401(k)
• Pension (Canada)
• Employee Stock Purchase Plan
• Mental Health Programs
• Flexible Schedules
• Paid Time Off
• Wellness Program
• Education Reimbursement
• Volunteer Opportunities
• Flexible Work Environment

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 750 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA today.