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Alcanza is seeking a Clinical Research Coordinator to support the execution of assigned studies at our Boston Clinical Trials site in Roslindale, MA. You will help screen participants, obtain consent, schedule follow-ups, and document data in source charts while maintaining GCP and FDA SOP compliance.
Responsibilities include data entry in EDC, collecting vital signs and ECGs, and supporting the site team in daily operations to ensure study integrity and participant safety.
Department: Operations
Employment Type: Full Time
Location: Boston Clinical Trials | Roslindale, MA
Reporting To: Rebecca Carrillo
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.
Essential Job Duties: In collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to: