Remote Ophthalmology Clinical Research Associate

Parexel; Cheyenne (WY); On-site; USD 90,000 - 110,000; Full time

Benefits offered by this job

Health Insurance

Tuition Reimbursement

Vacation/Holiday/Sick Time

401(k) with Company match

Flexible Spending & Health Savings

Work/Life Balance

Pet Insurance

Job summary

Parexel is seeking a Clinical Research Associate (CRA) with Ophthalmology monitoring experience to join our team. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and data integrity.

You will conduct onsite monitoring activities, build relationships with investigators, support enrollment and study delivery, and advance your career through Parexel's

Qualifications

• At least 18 months of direct onsite monitoring experience as a CRA.
• Ophthalmology clinical trial monitoring experience.
• Bachelor's degree or equivalent in biological science, pharmacy, or another health-related discipline.
• Knowledge of Good Clinical Practice and regulatory requirements.
• Experience using CTMS/EDMS and MS Office applications.

Responsibilities

• Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV), and termination visits (TV) at assigned clinical sites, and prepare timely visit and contact reports.
• Manage site quality and delivery from site identification through closeout.
• Serve as the primary point of contact for assigned clinical sites, addressing questions and resolving issues to support successful study execution.
• Oversee study integrity and build effective relationships with investigators and site staff.
• Review trial performance at designated sites and safeguard participant rights, safety, and well-being.
• Develop patient recruitment strategies with clinical sites to support enrollment timelines.
• Ensure compliance with SOPs, study protocols, amendments, GCP, and regulatory requirements.
• Evaluate data quality and site performance; verify investigational product accountability.
• Monitor the completeness and quality of regulatory documentation and perform site document verification.

Skills

Site relationship mgmt

Problem solving

Communication

Multitasking

Education

Bachelor's degree in biological science, pharmacy, or health-related discipline

Tools

CTMS

EDMS

Microsoft Office (Excel/Word)

Job description

Parexel is seeking a Clinical Research Associate (CRA) with Ophthalmology monitoring experience to join our team. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and data integrity.

You will conduct onsite monitoring activities, build relationships with investigators, support enrollment and study delivery, and advance your career through Parexel's