Clinical Research Associate, CRA II/Senior – Ophthalmology

Parexel

. Manage clinical sites from identification through closeout .

Posted 9/21/2026full-timeRemote • United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical sites, ensuring compliance with Good Clinical Practice and regulatory requirements, and fostering strong relationships with site staff and investigators. Proficient in utilizing Clinical Trial Management Systems and Electronic Document Management Systems to support study execution and data integrity.

Highest-signal resume keywords

Clinical Research Associate ExperienceOphthalmology Clinical Trial MonitoringGood Clinical Practice KnowledgeClinical Trial Management System ExperienceSite Relationship Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Onsite Monitoring ExperiencePatient Recruitment StrategiesData Quality EvaluationSite Document VerificationRegulatory Documentation Monitoring

Soft Skills

Problem-Solving SkillsCommunication SkillsInterpersonal SkillsOrganizational SkillsClient-Focused Approach

Tools & Technologies

Clinical Trial Management SystemElectronic Document Management SystemMicrosoft Office Applications

Industry Keywords

Clinical TrialsStudy ProtocolsRegulatory RequirementsGood Clinical PracticeBiological Science

About the role

Key responsibilities & impact

Manage clinical sites from identification through closeout
Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites
Prepare timely visit and contact reports
Serve as the primary point of contact for assigned clinical sites
Address site questions and resolve issues to support successful study execution
Oversee study integrity and build relationships with investigators and site staff
Review trial performance and safeguard study participants’ rights, safety, and well-being
Develop patient recruitment strategies with clinical sites to support enrollment timelines
Ensure compliance with standard operating procedures, study protocols and amendments, Good Clinical Practice, and applicable regulatory requirements
Evaluate reported data quality and integrity, site performance, and investigational product accountability
Monitor regulatory documentation completeness and quality
Perform site document verification

Requirements

What you’ll need

At least 18 months of direct onsite monitoring experience as a Clinical Research Associate
Ophthalmology clinical trial monitoring experience
Bachelor's degree or equivalent in biological science, pharmacy, or another health-related discipline
Knowledge of Good Clinical Practice, applicable regulatory requirements, and clinical trial processes
Experience using a Clinical Trial Management System
Experience using an Electronic Document Management System
Experience using Microsoft Office applications, including Excel and Word
Strong site relationship management, problem-solving, and communication skills
Ability to work independently with urgency and limited oversight
Client-focused, flexible approach to assignments and continuous learning
Ability to manage multiple priorities, evaluate changing scenarios, apply study protocols, and meet project timelines
Ethical, patient-focused approach and strong attention to quality and detail
Comfort collaborating within a matrixed team and communicating clearly with internal and external stakeholders
Strong interpersonal, written, verbal, organizational, and problem-solving skills

Benefits

Comp & perks

Health, Vision & Dental Insurance
Tuition Reimbursement
Vacation/Holiday/Sick Time
Flexible Spending & Health Savings Accounts
Work/Life Balance
401(k) with Company match
Pet Insurance
Paid time off
Life insurance
Additional benefit offerings in accordance with applicable plan terms
Some roles may be eligible for additional incentives, bonuses, or other compensation programs