Dson Connected: Clinical Research Coordinator (Full-time)
Christine Talbot ‘13, Clinical Neuropsychometrician at Boston Center for Memory, shared this opportunity and has offered to serve as a resource to interested Dickinsonians! Christine can be contacted at christine@bostonmemory.com.
Boston Center for Memory is an independent multi-specialty diagnostic and treatment center. We provide comprehensive diagnostic evaluations with a specialized treatment plan, recommendations, and continuing follow up care for memory disorders, including Mild Cognitive Impairment, Alzheimer’s disease and other related dementias. The Boston Center for Memory also conducts clinical research evaluating medications, vaccines, and testing instruments.
This opportunity may interest a recent Dickinson grad who wants to contribute to Alzheimer's clinical trials in a small company setting.
Clinical Research Coordinator (Full-time)
Job Description
The Clinical Research Coordinator (CRC) is responsible for overseeing and managing industry sponsored clinical protocols. The CRC will provide technical, administrative, and research support to the principal investigator, sub-investigators and collaborate with the research staff. The CRC is also has responsibility for completing various tasks including data collection, data submission, adverse event reporting, patient scheduling, registration and follow-up, records management, protocol regulatory management, quality assurance and other activities related to research project coordination. The CRC will interact with patients and their caregivers and our clinical team including neurology, psychiatry, and neuropsychology.
Responsibilities
- Identify, schedule and/or conduct participant study visits, tests and/or interviews/telephone follow up calls
- Ensure accuracy and completion of all regulatory documentation, including local or central IRB and study data
- Conduct preliminary quality assurance reviews of study data
- Present study status reports related to assigned research projects
- Track and maintain study related information in the data management system within the required timeframe
- Responsible for monitoring the inventory of research related supplies
- Ensure clinicians and/or PI accurately document their study activities according to protocol.
- Monitor strict adherence to all study protocols, including all regulatory requirements adhering to appropriate federal, local and institutional guidelines.
- Comply with all safety and infection control standards appropriate to this position
- Adhere to Good Clinical Practice (GCP) guidelines and all human subject protection practices
Basic Requirements
- Bachelor’s degree, registered nursing degree, or equivalent research experience
- Minimum one year experience coordinating clinical trials
- Experience with industry sponsored clinical trials and/or research in a medical setting is preferred
- Must be proficient with MS Office Suite, including Excel, Word
Preferred Skills
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 participants, and clinicians; and demonstrate competence in adhering to research ethics, IRB procedures, and other regulatory policies.
Competitive compensation package and position level will be commensurate with experience, background, and education.
Please send your resume/CV to info@bostonmemory.com.