Clinical Research Nurse

Preferred Oncology Experience Job Summary

With principal investigator oversight, prepares, evaluates and implements research studies to enhance the advancement of clinical practice.

• Serves as primary coordinator / project manager on a variety of research studies with low or moderate regulatory, clinical, and operational complexity; supports the PI and research team members.
• Evaluates and prepares research studies for implementation including: assessment of operational feasibility; budget development; preparation of IRB documents; institutes protocol operations (generation of data collection tools, case report forms); attends study meetings.
• Identifies, recruits, screens, assesses eligibility, and enrolls subjects per protocol; with appropriate training and delegation, performs protocol-required research activities.
• Assess patient status; collects, reviews, and documents data into a variety of systems per protocol.
• Assesses, plans, implements and evaluates educational programs, procedure and protocol updates to meet the identified needs of physician investigators, nursing staff, program staff, patients, family and/or the community.
• Maintains research studies in compliance with federal, state, and local law, GCP, contracts, and institutional policies.
• Coordinates and/or performs study activities which may include: respiratory therapy assessments; identification of adverse events; investigational product/test article (drug or device) accountability and administration; collection, processing, and shipment of research specimens; and other research activities to the extent permitted by law and policy.
• Communicates, collaborates, networks, and acts as a consultant to the study sponsor and/or CRO, research study centers, academic institutions, investigators, physicians/physician offices, ancillary departments, and the multidisciplinary team (including students and residents).

• Bachelor's Degree or equivalent in a health or science related field
• Registered Nurse (RN) - State of Michigan Upon Hire- REQUIRED
• Basic Life Support (BLS) - AHA American Heart Association 90 Days Or
• Basic Life Support (BLS) - ARC American Red Cross 90 Days
• Shipping and Handling of Specimen Training-Certification - 90 Days

• 1 year of relevant experience In clinical research and project management
• Adv Cardiovascular Life Support (ACLS) - AHA American Heart Association As Needed-required when indicated by the clinical trial protocol
• Pediatric Adv Life Support (PALS) - AHA American Heart Association As Needed-required when indicated by the clinical trial protocol

As a team member at Corewell Health, you will play an essential role in delivering personalized health care to our patients, members and our communities. We are committed to cultivating and investing in YOU. Our top‑notch teams are comprised of collaborators, leaders and innovators that continue to build on one shared mission statement - to improve health, instill humanity and inspire hope.

Join a nationally recognized health system with an ambitious vision of continued advancement and excellence.

• Comprehensive benefits package to meet your financial, health, and work/life balance goals. Learn more here.
• On‑demand pay program powered by Payactiv
• Discounts directory with deals on the things that matter to you, like restaurants, phone plans, spas, and more!
• Optional identity theft protection, home and auto insurance, pet insurance
• Traditional and Roth retirement options with service contribution and match savings
• Eligibility for benefits is determined by employment type and status

SITE - 25 Michigan St NE - Grand Rapids

Cancer Research Consortium West Mich - Grand Rapids Hosp

Full time

Day (United States of America)

40

8:30 a.m. to 5:00 p.m.

Monday to Friday

N/A

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