Clinical Research Coordinator I (Alzheimer's Research)
About The Position
The Kimberly Laboratory in the Center for Genomic Medicine (CGM) at Massachusetts General Hospital (MGH) is seeking a motivated, enthusiastic candidate to join our research group. Our research group investigates multiple neurologic disorders, including neurodegenerative diseases, stroke, and traumatic brain injury. The Clinical Research Coordinator I will support multiple ongoing clinical research studies focused on the use of novel portable, low-field MRI and blood biomarker discovery, with an emphasis on Alzheimer’s disease, in an outpatient clinic setting. This role involves coordinating participant recruitment and scheduling, obtaining informed consent, performing study-related tasks, managing regulatory documentation, and ensuring compliance across multiple protocols. The Clinical Research Coordinator I will be encouraged to complete phlebotomy training and will perform some wet bench work. The coordinator will also be responsible for ordering laboratory supplies, study-related equipment, and related financial and administrative tasks. This position involves working closely with an interdisciplinary team of investigators, physicians, nurses, industry partners, and suppliers to facilitate study operations. The position requires strong organizational skills, attention to detail, and comfort working directly with patient populations in a fast-paced research environment.
Requirements
- Bachelor's Degree Related Field of Study required
- Some relevant research project work 0-1 year preferred
- Careful attention to detail and good organizational skills.
- Ability to follow directions.
- Good interpersonal and communication skills.
- Computer literacy.
- Working knowledge of clinical research protocols.
- Ability to demonstrate respect and professionalism for subjects' rights and individual needs.
Responsibilities
- Coordinating participant recruitment and scheduling
- Obtaining informed consent
- Performing study-related tasks
- Managing regulatory documentation
- Ensuring compliance across multiple protocols
- Complete phlebotomy training
- Perform some wet bench work
- Ordering laboratory supplies
- Ordering study-related equipment
- Related financial and administrative tasks
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
