Senior Clinical Research Associate II – Ophthalmology

Fortrea

. Provide a high standard of care for participants in clinical trials and respond to emergency situations based on clinical research standards .

Posted 10/6/2026full-timeRemote • United StatesSenior💰 $125,000 - $142,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Clinical Monitoring and Oncology, ensuring compliance with clinical research standards and effective management of study sites. Proficient in data integrity verification and Serious Adverse Event reporting while maintaining strong teamwork and communication skills.

Highest-signal resume keywords

Clinical Monitoring ExperienceOncology ExperienceData Management Systems ProficiencySerious Adverse Event ReportingTeamwork and People Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementData Integrity VerificationCase Report Form ReviewProtocol ComplianceFeasibility AssessmentEmergency ResponseStudy Site MonitoringInformed Consent ProceduresTraining and Co-MonitoringProject Coordination

Soft Skills

TeamworkCommunicationAdaptabilityAttention to DetailProblem-Solving

Tools & Technologies

FortreaData Collection ToolsComputer Software

Certifications & Qualifications

Nursing LicensureAllied Health Certification

Industry Keywords

Clinical ResearchOncologyClinical TrialsRegulatory CompliancePatient Enrollment

About the role

Key responsibilities & impact

Provide a high standard of care for participants in clinical trials and respond to emergency situations based on clinical research standards
Conduct all aspects of study site monitoring, including routine monitoring and close-out of clinical sites
Maintain study files and conduct pre-study and initiation visits
Liaise with vendors
Manage study sites according to project plans
Ensure study staff receive proper materials and instructions to safely enroll patients
Verify informed consent procedures and protocol requirements comply with applicable regulations
Ensure integrity of data submitted on Case Report Forms and other data collection tools
Monitor data for missing or implausible data
Manage registries and undertake feasibility work when requested
Complete Serious Adverse Event reporting, reports, narratives, and follow-up
Perform CRF review and query generation and resolution in Fortrea or client data management systems
Assist with training new employees through co-monitoring
Coordinate designated clinical projects as a Local Project Coordinator
Act as a local client contact when assigned
Perform other duties assigned by management

Requirements

What you’ll need

Residing on the East Coast of the US
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
5+ years of Clinical Monitoring experience
Oncology experience preferred, especially early phase
30-50% overnight travel
Ability to work in a fast-paced, changing-priority, technology-based environment
Teamwork and people skills
Ability to sit for extended periods and operate a vehicle safely
Repetitive hand movement of both hands and ability to make fast, simple, repeated movements of the fingers, hands, and wrists
Occasional crouching, stooping, frequent bending and twisting of upper body and neck
Ability to access and use a variety of computer software
Light to moderate lifting and carrying of objects, luggage, and laptop computer, up to 15-20 lbs
Regular and consistent attendance
Varied hours may be required

Benefits

Comp & perks

Remote work arrangement
Ongoing application acceptance