Sr. Clinical Research Coordinator (Psychiatry and Behavioral Sciences)
About The Position
Bayview Geriatric & Neuropsychiatry is seeking a Sr. Clinical Research Coordinator to oversee the day-to-day activities of a single complex study or multiple clinical research studies and make independent decisions that impact the conduct of research. The role assists in goal setting and creating implementation plans, and contributes to budget formulation, communications, and data systems. The coordinator supports operational planning and study design, develops study procedures and materials, helps manage regulatory compliance, recruitment, budgets, and data systems, and participates in study meetings and reporting. The role also oversees collection and shipment of blood to a national repository and conducts comprehensive clinical and cognitive assessments of research participants in accordance with study protocols and standardized procedures.
Requirements
- Bachelor's degree in a related field.
- Three years of related experience.
- Additional education may substitute for required experience, and additional related experience may substitute for required education beyond a high school diploma or equivalent, to the extent permitted by the JHU equivalency formula.
Nice To Haves
- Master's degree in a related field.
- Proficiency in coordinating tasks across multiple research teams.
Responsibilities
- Assist the Principal Investigator or more senior research staff in ensuring the operational feasibility of proposed protocol or study designs.
- Develop standard operating procedures and data collection forms from protocols.
- Develop consent forms for clinical trials based on protocols.
- Prepare materials for submission to the Institutional Review Board (IRB).
- Contribute to work with commercial and/or government agency sponsors and recommend which group can commit, considering the patient population, available resources, and cost of providing services.
- Ensure compliance with protocols, procedures, and applicable regulations.
- Participate in developing the study budget.
- Develop and oversee implementation of recruitment strategies for participants in assigned studies.
- Set up a data collection system and ensure the validity of study data.
- Organize and quality control study data.
- Perform self-audits and/or audit other sites.
- Participate in study meetings, provide status updates, and recommend changes to protocol operations based on results and goals.
- Conduct literature searches to provide background information.
- Abstract and index information based on knowledge of the subject matter.
- Oversee collection and shipping of blood to a national repository.
- Conduct comprehensive clinical and cognitive assessments of research participants in accordance with study protocols and standardized procedures.
- Perform other duties as assigned.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
