Ophthalmic Clinical Research Coordinator

Panorama Eye Care LLC; Fort Collins (CO); On-site; USD 37,000 - 45,000; Full time

Benefits offered by this job

PTO accruals 3 weeks

Medical and dental insurance

Optical allowance

Routine eye care coverage

Disability insurances

Educational allowance

Paid holidays

401K with company match

Job summary

Panorama Eyecare in Fort Collins, CO seeks a Clinical Research Coordinator to manage ophthalmic clinical trials, ensure ethical study conduct, and support study teams.

The role emphasizes data integrity, protocol compliance, and collaboration with clinicians, sponsors, and staff. Requires attention to detail, MS Office skills, and relevant certifications. Full-time position with competitive hourly pay and growth opportunities.

Qualifications

• High school diploma or equivalent required.
• Experience utilizing Microsoft Office Applications (Outlook, Word, etc.).
• COA/COT and/or CCRC preferred; Certifications must be maintained.
• GCP certification maintenance required.
• Prior experience with human subjects.
• Prior research related experience preferred.
• Phlebotomy certification preferred.

Responsibilities

• Manage study patient care, educate participants, dispense study product, schedule visits.
• Promote and enroll clinical research patients into research program.
• Attend surgeries and guide ASC staff.
• Identify adverse events and follow reporting requirements.
• Receive, manage, and dispense investigational product; calibration checks.
• Track study supply inventory and re-orders as necessary.
• Attend investigator meetings and coordinate with sponsors/IRBs.
• Ensure logs and documentation are complete and compliant.
• Train staff on protocol requirements and changes.

Skills

Attention to detail

Microsoft Office proficiency

Clinical research mindset

Education

High school diploma or equivalent

Tools

Microsoft Office

GCP certification management

Phlebotomy certification (preferred)

Job description

Panorama Eyecare in Fort Collins, CO seeks a Clinical Research Coordinator to manage ophthalmic clinical trials, ensure ethical study conduct, and support study teams.

The role emphasizes data integrity, protocol compliance, and collaboration with clinicians, sponsors, and staff. Requires attention to detail, MS Office skills, and relevant certifications. Full-time position with competitive hourly pay and growth opportunities.