Clinical Research Coordinator

Work Status Details: REGULAR FULL TIME | 80.00 Hours Every Two Weeks
Pay Rate Type: Annual Salary
Listed is the base hiring salary range offered for this position. Actual salaries may vary depending on factors, including but not limited to skills and experience. The salary range listed is just one component of the total rewards/compensation package offered to candidates.
Min = $56,921.705
Mid = $71,152.131

SUMMARY:

The Clinical Research Coordinator coordinates with Principal Investigator (PI) and department to help ensure that Clinical Research and related activities are performed in accordance with federal regulations and YRMC institutional policies. This individual requires strong interpersonal skills, ability to communicate with patients regarding study risks and benefits, ability to educate patients, compassion and a desire to help people and uses strong communication skills, organizational skills, attention to detail. The Clinical Research Coordinator is responsible for the efficiency and accuracy of clinical studies through all stages as the study progresses and show vigilance in participant safety, protocol compliance, and data quality.

MINIMUM EDUCATION AND EXPERIENCE REQUIRED:

• Bachelor’s Degree and 2+ years related Clinical Research experience.
• BLS certified

Preferred Education and Experience:

• Certified phlebotomist or previous medical assistant experience
• Bilingual in Spanish and English
• Certification with SOCRA or ACRP

Why Yuma Regional Medical Center?
Yuma Regional Medical Center (YRMC) is located in Yuma, AZ. Our purpose is building a healthier tomorrow. We strive by putting patients first as they are the center of every decision and action we take. YRMC is rooted in the community by living and breathing the dynamic nature of our region. Being committed to progress by constantly and consistently advancing healthcare, creating meaningful experiences and improving the lives of everyone around us.
Our Values
Bring Kindness | Achieve Together | Aspire For Better | Do The Right Thing | Lead With Optimism |
About Yuma, AZ
Named by the Guinness World Records as the Sunniest City on Earth with winters averaging temperatures of 70 degrees, sunny days and cooler nights.
Yuma, Arizona is a place to explore the great outdoors with hiking, jet skiing, boating and off-roading. Don’t forget to soak up the sun at the great Colorado River or one of Yuma’s many lakes.
Yuma is centrally located in Southwest Arizona, within a short drive to many popular attractions and destinations.
https://www.visityuma.com/
https://www.yumachamber.org/
Bring your skills to one of the sunniest places on earth - Yuma, AZ!
Physical Requirements and working conditions for this position will be provided to you up on interview

Conducts all research related activities in compliance with institutional policies, good clinical practice, FDA, OHRP, and HIPAA policies.
Provides study start-up documents (paper or electronic) to Clinical Research Regulatory Coordinator. Supports the Clinical Research Regulatory Coordinator in the maintenance of regulatory documents in accordance with SOPs. Develops accurate source materials and ensures compliance from study team. Assist with the maintenance of subject logs, research charts and study binders.
Conducts recruitment activities. Monitors the study to ensure that it complies with protocols, is ethically conducted and follows regulatory standards. Coordinates and/or performs a variety of procedures/tests including, but not limited to, laboratory tests/phlebotomy, vital signs, ECG/EKGs, imaging studies, questionnaires/evaluations, as well as other needs as outlined in the study protocol(s). In accordance to job scope and responsibilities participates in the protocol specified study visit activities.
Assures collection, labeling, processing, storage and shipment of any protocol-required samples for local or central laboratory analysis. Maintains study supply inventory to include accountability and dispensing records.
Resolve research data queries within the SOP guidelines, Sponsor or CRO protocol and contract requirements. Collects and submits source data per protocol requirements while maintaining good documentation practices.
Assists in the preparation for and participates in the conduction of audits/monitoring visits as required.
Other duties as assigned.