Clinical Research Coordinator/ CTC Research / Full-Time

CHRISTUS Health • Santa Fe, NM

17h

About The Position

The Clinical Research Coordinator (CRC) is responsible for coordinating and collaborating with principle investigators on multiple ongoing research studies in an effort to facilitate research at CHRISTUS St. Vincent Health System. In addition to coordinating clinical care, they have a central role in assuring participant safety, maintenance of informed consent, integrity of protocol implementation as well as working closely with the principal investigator. While the Principal Investigator is ultimately responsible for the clinical trial, the CRC is responsible for the facilitation and coordination of the daily clinical trial activities and plays a critical role in the conduct of the study. The CRC works collaboratively with the entire CSV team, sponsors, and monitors to ensure productivity and timely completion of studies.

Requirements

• High School Diploma or equivalent required.
• Proficiency in using computer databases, spreadsheets and word processing software, and electronic health systems used in research environment, or have a willingness to learn and demonstrate proficiency within six months of hire
• Requires excellent oral and written communication skills
• Requires excellent organizational skills
• Proficient in organizing and examining data
• Must be able to produce clear and concise products
• Must be thorough in gathering and reporting information
• Must be flexible and be able to relate well with a variety of people
• Two years of experience healthcare.
• Certificate of training in Good Clinical Practice must be completed within 1 month of hire.

Nice To Haves

• Bachelor's Degree in Healthcare Administration, Research, Biology, Business or related field preferred.
• Phlebotomy certification preferred.

Responsibilities

• Coordinating clinical care
• Assuring participant safety
• Maintenance of informed consent
• Integrity of protocol implementation
• Facilitation and coordination of daily clinical trial activities
• Collaborating with the entire CSV team, sponsors, and monitors to ensure productivity and timely completion of studies.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED