Senior GI Clinical Trials Coordinator

Gastro Health; Olympia (WA); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Medical

Dental

401(k) retirement plan

Profit-sharing

Job summary

Gastro Health is seeking an industry professional to join our research team. This role will work directly with subjects under the PI and oversee all aspects of clinical research trials in line with FDA/ICH-GCP guidelines.

Responsibilities include coordinating site activities, ensuring subject safety, maintaining regulatory compliance, and data collection across studies with solid communication and organizational skills.

Qualifications

• Minimum of 2 years of clinical research experience required.
• Phlebotomy/Venipuncture experience preferred.
• Bachelor's degree preferred.
• SOCRA and/or ACRP certification preferred.

Responsibilities

• Coordinate site visits and monitor visits per protocol.
• Ensure safety and well-being of study subjects throughout participation.
• Maintain regulatory compliance with FDA and ICH-GCP guidelines.
• Record adverse events and manage data in source documents.
• Obtain IRB approvals prior to initiating activities.
• Recruit and track subjects to meet enrollment goals.

Skills

Clinical research experience

Phlebotomy

Strong communication

Self-starter

Travel willingness

Education

Bachelor's degree (preferred)

Tools

CTMS

EDC

IWRS/IXRS

EHR (AllScripts)

Job description

Gastro Health is seeking an industry professional to join our research team. This role will work directly with subjects under the PI and oversee all aspects of clinical research trials in line with FDA/ICH-GCP guidelines.

Responsibilities include coordinating site activities, ensuring subject safety, maintaining regulatory compliance, and data collection across studies with solid communication and organizational skills.