🧪 Job Title:
Ophthalmology CRA II & Senior CRAs – US
🏢 Company:
Fortrea
🌐 www.fortrea.com
📌 Job Information:
Job ID: 254315
Category: Clinical
Locations: Available in 14 U.S. locations (Open to major hub cities across the U.S.)
Work Style: Remote
Employment Type: Full-time or Part-time (20+ hours/week)
Salary Range: $105,000 – $140,000/year
Application Deadline: Ongoing
#LI-Remote
📋 Job Overview:
Fortrea is seeking experienced Clinical Research Associates (CRA II and Sr. CRA) with a strong background in ophthalmology studies to support its Full Service Outsourcing (FSO) team. You’ll lead and manage clinical site activities to ensure the safe, efficient, and compliant execution of clinical trials.
🧭 Key Responsibilities:
🔍 Site Monitoring & Management
Conduct site visits: pre-study, initiation, routine monitoring, and close-out
Maintain essential study documents and files
Ensure clinical site staff receive necessary training and protocol materials
Verify informed consent procedures and adherence to regulatory requirements
Monitor data quality and integrity from Case Report Forms (CRFs)
Generate and resolve queries per data review guidelines
📝 Reporting & Compliance
Complete Serious Adverse Event (SAE) reporting and follow-up narratives
Manage site registry requirements and perform feasibility assessments when required
Coordinate with vendors and internal stakeholders
Ensure study activities align with project plans and timelines
👩🏫 Team Support & Training
Assist with training and mentoring of new CRA team members
Participate in co-monitoring activities
May act as a Local Project Coordinator and/or local client liaison
🔄 Additional Duties
Support special projects and additional responsibilities as assigned by management
🎓 Qualifications:
Education:
University or college degree in a related field (e.g., nursing, pharmacy, life sciences)
Certification in an allied health profession from an accredited institution (e.g., nursing licensure)
Experience:
1–3+ years of clinical monitoring experience required
Ophthalmology clinical trial experience strongly preferred
Experience working in:
Fast-paced, high-regulatory environments
Electronic data capture and remote trial technologies
Teams with rapidly shifting priorities
💡 Key Competencies:
Excellent communication and interpersonal skills
Strong attention to detail and data accuracy
Ability to manage multiple priorities under tight timelines
Strong decision-making and problem-solving skills
Proficiency in electronic trial documentation and data systems
🎁 Benefits (Eligibility: 20+ hours/week):
Medical, Dental, Vision Insurance (multiple carriers)
Life Insurance, Short- and Long-Term Disability (STD/LTD)
401(K) Retirement Plan
Paid Time Off (PTO) – Flex Plan
Employee Recognition Awards
Access to Employee Resource Groups (ERGs)
🌍 Work Environment:
Remote / Home-based
May involve limited travel based on project requirements
📣 Why Fortrea?
Fortrea is a leading global CRO with clinical operations in ~100 countries, supporting development across 20+ therapeutic areas. We combine innovation, clinical rigor, and scientific expertise to bring life-changing treatments to patients faster.
Core Values – Fortrea FOUR:
Forward Together
Own It
Uphold Integrity
Respect People
Become part of a collaborative team focused on global health impact and personal growth.
⚖️ Equal Opportunity Employer:
Fortrea is committed to diversity, equity, and inclusion. Accommodations are available upon request.
🔗 Learn more about EEO & Accommodations
📬 Share this Opportunity:
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