Find Jobs
Find Jobs Near You – Available Work in Your Location
Skip to job details
BH
BAMF Health
Clinical Trials Research Coordinator
Career Insights for Clinical Research Coordinator
See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.
Scorecard
Based on Michigan data
Review key factors to help you decide if this role fits your goals. How is this calculated?
What they do
A Clinical Research Coordinator directs clinical research and development projects for companies, and coordinates testing and quality control.
$115,613 / year median in Michigan
+13% projected growth
Job Description
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 Coordinator (CRC) plays a pivotal role in conducting clinical trials focused on investigational PET tracer and radiopharmaceutical therapies. Works closely with a team of medical professionals and researchers to ensure our clinical trials are conducted efficiently, ethically, and within regulatory compliance. Responsible for managing all aspects of the clinical trials, from participant recruitment to data collection and analysis, ensuring the integrity and quality of the research. Duties and Responsibilities, including but not limited to: Coordinate and manage clinical trials from initiation to closure, including patient recruitment, screening, enrollment, and follow-up. Patient recruitment. Pre-screen potential candidates medical records for appropriateness for participation. Coordinate all necessary resources for successful conduct of clinical trial protocol, including: providers, clinic rooms, clinic staff, imaging equipment, radiopharmacy, etc. Maintain accurate and complete clinical trial documentation and records. Facilitate communication between the clinical site, research team, and sponsors. Train and oversee research staff and volunteers, as necessary. Manage the procurement, storage, and handling of study materials, including investigational products and radiopharmaceuticals. Ensure participant safety and confidentiality according to HIPAA regulations.