Clinical Research Coordinator — Multi-Site Trials & Compliance

alcanzaclinical; Boston (MA); On-site; USD 55,000 - 75,000; Full time

Job summary

Alcanza is a growing clinical research company with multiple sites across the United 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 collaborate with investigators to maintain study integrity, assist with regulatory documentation, and support patient recruitment across Phase I-IV trials, creating a high-quality, ethical research environment.

Responsibilities

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

Job description

Alcanza is a growing clinical research company with multiple sites across the United 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 collaborate with investigators to maintain study integrity, assist with regulatory documentation, and support patient recruitment across Phase I-IV trials, creating a high-quality, ethical research environment.