Clinical Research Coordinator: Lead Multi-Site Trials

alcanzaclinical; Town of Florida (NY); On-site; USD 52,000 - 76,000; Full time

Job summary

Alcanza is a growing clinical research company with a network of locations across multiple states. The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.

The CRC will contribute to study execution across Phase I-IV studies and various therapeutic areas, supporting the company's mission as it expands its multi-site operations.

Qualifications

• Experience ensuring study execution in compliance with GCP, ICH, HIPAA, FDA regulations and SOPs.

Responsibilities

• Ensure execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA regulations and SOPs.

Skills

GCP compliance

ICH guidelines

HIPAA

FDA regulations

SOP adherence

Job description

Alcanza is a growing clinical research company with a network of locations across multiple states. The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.

The CRC will contribute to study execution across Phase I-IV studies and various therapeutic areas, supporting the company's mission as it expands its multi-site operations.