What are the responsibilities and job description for the CRP - CLINICAL RESERACH COORDINATOR III position at MOUNTAIN VIEW HOSPITAL LLC?
Job Details
Description
Mountain View Hospital is looking for a Clinical Research Coordinator III to join our team!
JOB SUMMARY: Manages multiple clinical trials from start up through study close out in accordance with study protocols, GCPs, and SOPs. Interacts with Clinical Trial Monitors and other representatives from trial sponsors. Able to perform all the assigned tasks of a Clinical Research Coordinator.
BENEFITS:
Taking care for our community starts with taking care of our own team. Mountain View Hospital is proud to offer its employees competitive and comprehensive benefit packages. Benefits include:
- Medical, Dental and Vision Insurance
- Paid Time Off (vacation, holidays and sick days) and Medical Paid Time Off
- Retirement Plans (401K with up to 6% match)
- Earned Quarterly Bonus Program
- Education Reimbursement Program
- Discount for medically necessary procedures performed at Mountain View Hospital and Idaho Falls Community Hospital
- Life Insurance
- Short- and Long-Term Disability
- Flexible Spending Accounts
- Employee Assistance Program
- Flexible Schedules
- Collaborative and Supportive Work Environment
Please note benefits are based on eligibility according to full-time, part-time or PRN status classification.
ABOUT MOUNTAIN VIEW:
Mountain View Hospital and our 29 affiliate clinics are committed to providing compassionate, cutting edge care to our patients. We serve the entire Snake River Valley – all the way from Pocatello to Rexburg. Our medical capabilities span everything from wound care to urgent care, oncology to neurology, physical therapy to speech therapy, a Level III NICU, robust robotic surgery department and a continuously expanding rural health practice.
Our work environment is mission driven, people-centric and supportive. It is what sets apart and makes people excited to come to work each day. If you are looking for a career where you can make a difference in your community, we invite you to apply.
Qualifications
Education/Certification: High School Diploma or equivalent or higher. Current BLS Certification. Completion of Good Clinical Practice (GCP) training. Clinical Research Coordinator Certification through ACRP.
Experience: 2-years’ experience as a Clinical Research Coordinator. Participation in new study start up and study close out. Experience leading blinded and unblinded study teams.
Equipment/Technology: Experience with office equipment, medical equipment used to obtain vitals, computer systems to enter data and process information.
Language/Communication: Ability to read and communicate effectively in English. Bilingual is a plus. Must understand medical terminology.
Mathematical Skills: General math skills.
Mental Capabilities: Can regularly and consistently make sound judgments. Must be organized, attentive to details, critical thinker.
Interpersonal: Good communication skills, able and comfortable to collaborate with others to accomplish tasks.
Performance: Work well with deadlines and multiple projects simultaneously. Good customer service skills. Must maintain individual source accuracy and ICF Accuracy of 95%.
