Clinical Research Coordinator: Drive Patient-Centric Trials

Accel Research Sites; Massachusetts; Hybrid; USD 52,000 - 72,000; Full time

Job summary

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.

Qualifications

• Role ensures execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.

Responsibilities

• Screening of patients for study enrollment.
• Patient consents.
• Patient follow-up visits.
• Documenting in source clinic charts.
• Entering data in EDC and answering queries.
• Obtaining vital signs and ECGs.
• May perform.

Job description

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.