Panorama Eye Care LLC

Clinical Research Coordinator

Job Overview

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Employment Type

Full-time
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Compensation

Type:
Hourly
Rate:
Range $27.00 - $33.00
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Work Schedule

Standard Hours
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Benefits

Paid Time Off
Medical insurance
Dental Insurance
Optical allowance
Routine eye care
Short term disability insurance
long term disability insurance
Educational Allowance
Paid holidays
401K with company match

Job Description

Panorama Eyecare is a distinguished eyecare provider that prides itself on fostering a community of dedicated professionals committed to delivering the highest quality eyecare services. With a mission centered around excellence and patient-centered care, Panorama Eyecare stands out as an Employer of Choice by cultivating an environment of partnership, engagement, stewardship, and mutual respect. This organization is deeply invested in the professional growth and success of its team members, offering comprehensive training, ongoing support, and opportunities for career advancement. Operating from their clinic location, the Eye Center of Northern Colorado - Precision in Fort Collins, CO, Panorama Eyecare offers a... Show More

Job Requirements

  • High school diploma or equivalent required
  • experience utilizing Microsoft Office applications including Outlook and Word
  • COA, COT, and/or CCRC certifications preferred and must be maintained
  • good clinical practice certification maintenance required
  • prior experience with human subjects
  • prior research related experience preferred
  • phlebotomy certification preferred

Job Qualifications

  • High school diploma or equivalent
  • experience with Microsoft Office applications including Outlook and Word
  • prior experience working with human subjects in clinical research
  • preferred certifications include Certified Ophthalmic Assistant, Technician, or Clinical Research Coordinator
  • maintenance of applicable certifications required
  • prior research-related experience is preferred
  • phlebotomy certification is preferred
  • good communication and teamwork skills
  • ability to learn and apply clinical protocols
  • attention to detail and accuracy

Job Duties

  • Perform study related testing for clinical trial patients
  • educate and obtain consent from study participants
  • dispense study products according to protocol
  • schedule patient visits and manage study calendars
  • complete and maintain accurate source documentation
  • distribute stipends to study participants
  • communicate effectively with clinical trial participants and healthcare team
  • promote and enroll patients into research programs
  • attend study surgeries and provide guidance to Ambulatory Surgery Center staff
  • identify and report adverse events and serious adverse events
  • receive, manage, and dispense investigational products
  • conduct calibration checks on study equipment
  • track and reorder study supplies as needed
  • attend periodic investigator meetings
  • facilitate communication between Eye Center of Northern Colorado and sponsors, institutional review boards, and laboratories
  • capture detailed and accurate source information
  • perform data entry for all clinical studies
  • assist study monitors with data review and query resolution
  • ensure completion of study logs in a timely manner
  • train study and clinic staff on protocol requirements and changes
  • maintain the highest level of protocol compliance
  • obtain and maintain Certified Clinical Research Coordinator certification within 30 months of employment
  • maintain Good Clinical Practice certification
  • coordinate scheduling needs with other departments
  • perform additional duties as required
  • develop additional skills as necessary for study execution
  • exhibit high attention to detail and accuracy

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Job Qualifications

Experience

Mid Level (3-7 years)

Job Location

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