Clinical Research Coordinator - Research

Providence • Kennewick, WA

1d

About The Position

Clinical Research Coordinator 2 functions under the supervision of the Clinical Trials Manager. Exhibits increased productivity and independence relative to the clinical research coordinator 1 position. Coordinates and maintains diverse activities in the conduct of clinical research trials related to heart and vascular research. The coordinator establishes good working relationships with principal investigators, monitors, teammates, other departments and clinics to ensure timely study completion. Acts as liaison to Regional Research for budget and regulatory documents, and investigational drug services as needed. Assures protocol adherence, screens and recruits study subjects, obtains informed consent, conducts study visits and phone calls, maintains documentation, study materials and study products. Coordinator is responsible for the timely and accurate completion of source documents, case report forms and query resolution. Communicates frequently regarding progress of ongoing trials. Coordinates monitor visits. All study related activities will be conducted in compliance with the Code of Federal Regulations- GCP guidelines. Join our team at Kadlec Regional Medical Center where you’ll support nurses both in and out of surgery, among other patient care tasks. As a Providence caregiver, you’ll apply your specialized training to deliver world-class health with human connection and make a difference every day through your extraordinary care.

Requirements

• Bachelor's Degree in health-related field or equivalent education/experience
• Associate's Degree with courses related to healthcare, science or research or equivalent education/experience
• No degree: 2 years of clinical research experience
• Driving may be necessary as part of this role upon request. Caregivers are required to comply with all state laws and requirements for driving. Caregivers will be expected to provide proof of driver license and auto insurance upon request. See policy for additional information.
• 2 years clinical research work experience; supporting all aspects of clinical research

Nice To Haves

• Experience with electronic medical records and remote data capture

Responsibilities

• Coordinates and maintains diverse activities in the conduct of clinical research trials related to heart and vascular research.
• Establishes good working relationships with principal investigators, monitors, teammates, other departments and clinics to ensure timely study completion.
• Acts as liaison to Regional Research for budget and regulatory documents, and investigational drug services as needed.
• Assures protocol adherence, screens and recruits study subjects, obtains informed consent, conducts study visits and phone calls, maintains documentation, study materials and study products.
• Responsible for the timely and accurate completion of source documents, case report forms and query resolution.
• Communicates frequently regarding progress of ongoing trials.
• Coordinates monitor visits.
• All study related activities will be conducted in compliance with the Code of Federal Regulations- GCP guidelines.

Benefits

• Our best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally and achieving financial security. We take care of you, so you can focus on delivering our mission of providing safe, compassionate care.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 501-1,000 employees