Clinical Research Nurse
Join BAMF Health, where you're not just part of a team; you're at the forefront of a revolution in Theranostics, changing lives for the better. As a member of our global team, you'll contribute to pioneering technology and deliver top-tier patient care.
Located in the heart of downtown Grand Rapids, our cutting-edge global headquarters resides within the state-of-the-art Doug Meijer Medical Innovation Building. Step into our modern and spacious facilities, where innovation thrives and collaboration knows no bounds. Join us in our mission to make Theranostics accessible and affordable for all, and be part of something truly remarkable at BAMF Health. The Clinical Research Nurse is a critical member of the clinical trials team, responsible for the end-to-end coordination and execution of clinical research studies. This role combines clinical expertise with a strong understanding of research protocol requirements to ensure safe, ethical, and high-quality delivery of clinical trials across a variety of therapeutic areas. Working in close partnership with principal investigators, clinical trial coordinators, physicians, and multidisciplinary care teams, the Clinical Research Nurse ensures the seamless integration of research protocols into clinical practice. This includes managing day-to-day research operations such as participant screening, informed consent, data collection, investigational product management, and regulatory documentation. This role acts as both a patient advocate and protocol champion-ensuring participants are informed, supported, and safe throughout the study, while upholding strict adherence to Good Clinical Practice (GCP), institutional policies, and regulatory guidelines. Duties and Responsibilities, including but not limited to:- Serves as primary research nurse coordinator on a variety of research studies with moderate to high regulatory, clinical, and operational complexity; supports the principal investigator and research operations.
- Coordinates and/or performs study activities which may include nursing assessments, identification of adverse events, investigational product accountability and management, collection, processing, and shipment of research specimens, and other research activities to the extent permitted by law and policy.
- Identifies, recruits, screens, assess eligibility, and enrolls subjects per protocol.
- Maintains relationships with BAMF Health and external health care providers for the purposes of participant recruitment and coordination of care relative to research studies.
- Acts as a primary point of contact for the sponsor, CRO, and the clinical trial subjects.
- Maintain accurate and complete clinical trial documentation and records.
- Ensure participant safety and confidentiality according to HIPAA regulations.
- Train and oversee research staff and volunteers, as necessary.
- Associates degree or higher required
- Licensed RN in the State of Michigan required
- 2 years of work in a healthcare setting as a RN required
- Basic Life Support (BLS) - AHA or ARC, required upon hire
- Bachelor's degree or equivalent in a health or science related field preferred
- 1 year of relevant experience in clinical research preferred
- Experience in oncology, nuclear medicine, and/or radiology nursing preferred
- Advance Cardiac Life Support (ACLS) preferred
- OCN preferred
- SOCRA or ACRP certification preferred
- Employment Status: Full time (1.0 FTE)
- Weekly Scheduled Hours: 40
- Hours of work: Hours vary between 8:00 a.m. to 4:30 p.m.
- Days worked: Monday to Friday
- Employer paid High Deductible Health Plan with employer HSA contribution
- Flexible Vacation Time
- 401(k) Retirement Plan with generous employer match
- Several benefit options including, but not limited to; dental, vision, disability, life, supplemental coverages, legal and identity protection
- Free Grand Rapids downtown parking
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