🧪 Job Title:
Ophthalmology CRA II & Senior CRAs – West Coast
🏢 Company:
Fortrea
🌐 www.fortrea.com
📌 Job Information:
Job ID: 252868
Category: Clinical
Locations: Available in 14 U.S. locations (West Coast preferred)
Work Style: Remote
Employment Type: Full-time or Part-time (20+ hours/week)
Salary Range: $105,000 – $140,000/year
Application Deadline: Ongoing (applications accepted continuously)
📋 Job Overview:
Fortrea is seeking experienced Ophthalmology Clinical Research Associates (CRA II or Sr. CRA) to support its Full Service Outsourcing (FSO) team. This role involves monitoring, managing, and coordinating clinical trial activities in accordance with GCP, protocol requirements, and regulatory standards, primarily for ophthalmology-focused studies.
🧭 Key Responsibilities:
🔍 Monitoring & Site Management
Conduct all types of site visits (pre-study, initiation, monitoring, and close-out)
Ensure site compliance with protocols, informed consent, and regulatory guidelines
Monitor subject safety and verify data integrity (CRFs vs. source documentation)
Manage study files and perform data review, query generation, and resolution
Support Serious Adverse Event (SAE) reporting and follow-up
📊 Project Coordination & Oversight
Serve as Local Project Coordinator (as assigned)
Act as a local point of contact for client communications
Liaise with vendors and internal teams as per project needs
Conduct feasibility assessments when requested
👩🏫 Training & Mentorship
Assist with training and co-monitoring of new team members
🧠 Other Duties
Perform all additional tasks assigned by management
Maintain quality standards and timelines in a high-paced environment
🎓 Qualifications:
Education:
University/college degree or certification in a relevant health profession (e.g., nursing, life sciences, pharmacy) from an accredited institution
Experience:
1–3+ years of clinical monitoring experience
Previous experience in Ophthalmology clinical trials is strongly preferred
Comfortable working in:
Fast-paced, highly regulated environments
Tech-driven platforms (electronic data capture, remote monitoring, etc.)
Cross-functional and team-based structures
💡 Skills & Attributes:
Exceptional organizational and communication skills
Strong analytical and clinical judgment capabilities
Ability to prioritize and adapt quickly to changing needs
Detail-oriented with a commitment to data integrity and regulatory compliance
Comfortable with technology and electronic documentation tools
🎁 Benefits (Eligibility: 20+ hours/week):
Medical, Dental, Vision Insurance (multiple carriers)
Life Insurance, Short/Long-Term Disability (STD/LTD)
401(K) Retirement Plan
Paid Time Off (PTO) via Flex Plan
Employee Recognition Awards
Multiple Employee Resource Groups (ERGs)
🌍 Work Environment:
Remote / Home-based
Occasional travel may be required for site visits or meetings
📣 Why Fortrea?
Fortrea is a global Contract Research Organization (CRO) with operations in 100+ countries, offering end-to-end clinical development services. With deep therapeutic expertise across 20+ therapeutic areas, Fortrea is redefining the drug development landscape with speed, precision, and compassion.
Core Values – Fortrea FOUR:
Forward Together
Own It
Uphold Integrity
Respect People
Join a collaborative environment where innovation thrives and your contributions drive global health impact.
⚖️ Equal Opportunity Employer:
Fortrea is committed to creating a diverse and inclusive environment. Reasonable accommodations are available upon request.
🔗 Learn more about EEO & Accommodations
📬 Stay Connected:
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