CRC- Clinical Research Coordinator

Accel Research Sites

Massachusetts

On-site

USD 52,000 - 72,000

Full time

14 days+

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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

CRC- Clinical Research Coordinator

Department: Operations

Employment Type: Full Time

Location: Boston Clinical Trials | Roslindale, MA

Reporting To: Rebecca Carrillo


Description

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.


Key Responsibilities

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:

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