Clinical Research Coordinator I

Job Description:

Job Essentials

• Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out.
• Determine eligibility of and gather consent from study participants according to protocol. Assist with recruitment strategies.
• Coordinate collection of study specimens and processing.
• Collect and manage study participants, imaging, study drug accountability, and laboratory data for research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms.
• Ensure compliance with research protocols, and review case report forms for completion and accuracy with source documents.
• Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend regular meetings with staff/principal investigator, acting as primary contact.
• Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.
• Ensure essential documentation and recording of participant and research data in appropriate files per institutional and regulatory requirements.
• Participate in monitoring visits and regulatory audits.
• Work closely with internal departments such as radiology, pharmacy, and laboratory to schedule research activities for patients
• Collaboration with team members
• -Other duties may also be assigned

Minimum Qualifications

• Three years of clinical research experience worked with human subjects.

OR

• BA degree and 1 year if clinical research experience working with human subjects.

OR

• Professional certifications such as the CCRP (Certified Clinical Research Professional- SoCRA), CCRC (Certified Clinical Research Coordinator - ACRP), CIRB Certified Institutional Review Board professional or CRA Certified Research Administrator - which require 2 years of research experience and a test.

• Experience using basic computer programs including word processing, database, spreadsheet applications and e-mail.
• Experience using laboratory protocol, systems and documentation techniques.

Preferred Qualifications

• Bachelor's Degree or higher from an accredited institution.
• Prior experience in healthcare setting working directly with patients
• Expertise or prior experience in Hepatology, Gastroenterology, Abdominal Transplant
• Prior experience with electronic medical records systems
• Prior experience with Microsoft Office applications
• Strong interpersonal skills
• Knowledge of medical terminology

Physical Requirements:

Interact with others by effectively communicating, both orally and in writing.
- and -
Operate computers and other office equipment requiring the ability to move fingers and hands.
- and -
See and read computer monitors and documents.
- and -
Remain sitting or standing for long periods of time to perform work on a computer, telephone, or other equipment.
- and -
May require lifting and transporting objects and office supplies, bending, kneeling and reaching.

Location:

Work City:

Work State:

Scheduled Weekly Hours:

The hourly range for this position is listed below. Actual hourly rate dependent upon experience.

We care about your well-being - mind, body, and spirit - which is why we provide our caregivers a generous benefits package that covers a wide range of programs to foster a sustainable culture of wellness that encompasses living healthy, happy, secure, connected, and engaged.

Learn more about our comprehensive benefits packages for our Idaho, Nevada, and Utah based caregivers, and for our Colorado, Montana, and Kansas based caregivers; and our commitment to diversity, equity, and inclusion.

Intermountain Health is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

All positions subject to close without notice.