We are looking for a Clinical Research Coordinator to join our team.
This clinical research coordinator (CRC) position is at the Boston Center for Memory (BCM), a diagnostic, treatment, and research center in the greater Boston area. BCM conducts Phase II and Phase III clinical trials evaluating diagnostic measures, symptomatic treatments, and disease modifying treatments for Mild Cognitive Impairment, Alzheimer’s disease, and related dementias. The studies conducted at BCM are primarily industry funded, privately funded or investigator sponsored. We receive patients from the greater Boston area, including Cape Cod, Maine, NH, NY, RI, and VT.
The CRC’s principal duties involve coordinating one or more clinical protocols. The CRC will provide technical, administrative, and research support to the principle and sub-investigators. The CRC will help develop the intervention materials; accurately and reliably administer and score psychological assessments; coordinate with the interdisciplinary treatment teams to schedule patients; collaborate with the data coordinator to enter data into a central database; coordinate meetings, travel, and other study-related activities; and collaborate with the regulatory coordinator to manage regulatory reports and institutional review board (IRB) submissions. The CRC may provide guidance and supervision of research assistants.
Minimum Qualifications Bachelor’s degree, registered nursing degree, or equivalent research experience. At least 2 years of experience as a research assistant or research coordinator.
Experience with industry sponsored clinical trials and/or research in a medical setting is preferred. Must be proficient with MS Office Suite, including Excel, and Word.
Preferred Qualifications The successful CRC will have excellent organizational skills; impeccable accuracy and attention to detail; excellent time-management skills; an ability to work independently and with good judgment; an ability to professionally and effectively communicate with investigators, research subjects, and clinicians; and a demonstrate competence in adhering to research ethics, IRB procedures, and other regulatory policies. To apply, please email a cover letter and resume/CV, as well as the names and contact information of three professional references to email@example.com.