Lead Clinical Research Coordinator

2 weeks ago


Richmond, Virginia, United States Commonwealth of Virginia Full time
Commonwealth of Virginia - Institute for Drug and Alcohol Studies


The Commonwealth of Virginia is committed to fostering a diverse and inclusive workforce. We invite qualified candidates to consider the opportunity to join our team as a Senior Clinical Research Coordinator. This role is essential in advancing our mission to conduct impactful research in the field of substance use disorders and related neurobehavioral conditions.

As a Senior Clinical Research Coordinator, you will play a pivotal role in overseeing various clinical research trials. Your responsibilities will encompass all facets of the research process, including data collection, analysis, and dissemination of findings in collaboration with project investigators and team members. You will also supervise research assistants and student workers, ensuring that all research activities align with regulatory standards and best practices.

Key Responsibilities:

Maintain a comprehensive understanding of clinical research management from initiation to completion. Ensure compliance with all IRB requirements and human subjects protection regulations. Manage a portfolio of clinical research studies, ensuring adherence to timelines and deliverables. Provide training and mentorship to research assistants and student researchers. Develop and implement best practice guidelines for clinical research coordination. Oversee the preparation and submission of IRB documentation. Facilitate participant screening, enrollment, and testing as authorized by the Principal Investigator. Organize and lead meetings, ensuring effective communication among team members.
Minimum Qualifications:
A commitment to promoting a diverse and inclusive environment. A Bachelor’s degree or an equivalent combination of education and experience. A minimum of three years of experience in clinical trial coordination and regulatory affairs. Strong communication, organizational, and time management skills. Proficiency in data management and analysis tools.
Preferred Qualifications:
Experience in research administration and grant management. Familiarity with IRB policies and human research regulations. Advanced degree or relevant certifications in clinical research. Experience working with populations affected by mental health or substance use disorders.
Join us in making a difference through research and innovation. Your expertise will contribute to the advancement of knowledge and practices in the field of addiction studies.

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