Job Title: Clinical Research Associate II (CRA II) – Ophthalmology | Multiple U.S. Hub Locations
Location: Available in 15 U.S. Hub Locations (East Coast & West Coast)
Job Category: Clinical Research / Clinical Operations
Employment Type: Full-Time
Experience Required: 1–3 years of clinical monitoring experience (Ophthalmology required)
Travel Requirement: 60–70% travel | 8–10 Days On-Site (DOS) per month
Compensation: Target Pay Range: $105,000 – $117,000 annually
Application Status: Open – Applications accepted on an ongoing basis
About the Organization
Join Fortrea, a leading global Contract Research Organization (CRO) delivering clinical development and technology solutions across more than 20 therapeutic areas. Operating in approximately 100 countries, Fortrea partners with pharmaceutical, biotechnology, and medical device companies to advance innovative therapies from early development through commercialization.
Fortrea’s Full Service Outsourcing (FSO) team is actively seeking experienced Ophthalmology-focused Clinical Research Associate II (CRA II) professionals to support and lead clinical monitoring activities across multiple U.S. hub locations.
Position Overview
The Ophthalmology CRA II will independently manage and monitor clinical trial sites, ensuring protocol compliance, regulatory adherence, patient safety, and data integrity. This role requires therapeutic expertise in ophthalmology trials and the ability to manage site performance within a high-performance, compliance-driven environment.
The ideal candidate has hands-on ophthalmology monitoring experience and is comfortable with travel-intensive assignments while maintaining exceptional quality standards.
Key Responsibilities
Conduct all aspects of site monitoring, including pre-study visits, site initiation visits (SIV), routine monitoring visits (RMV), and close-out visits (COV)
Oversee comprehensive site management in alignment with project plans and timelines
Ensure site personnel are adequately trained and equipped to execute study protocols
Verify informed consent procedures and confirm adherence to regulatory and ethical requirements
Review source documentation and Case Report Forms (CRFs) to ensure accuracy, completeness, and data integrity
Identify missing or inconsistent data and generate/resolve queries within sponsor or internal data management systems
Manage registry activities and perform site feasibility assessments as required
Oversee Serious Adverse Event (SAE) reporting, including narrative preparation and follow-up
Liaise with vendors and cross-functional clinical teams
Support onboarding and co-monitoring of new CRAs
Serve as Local Project Coordinator when assigned, acting as a local client contact
Maintain essential regulatory documentation in accordance with ICH-GCP guidelines
Required Qualifications
University or college degree in life sciences, healthcare, or related discipline; or certification in an allied health profession (e.g., nursing licensure) from an accredited institution
1–3 years of independent clinical monitoring experience
Mandatory experience monitoring Ophthalmology clinical trials
Strong knowledge of ICH-GCP, FDA regulations, and global clinical trial standards
Willingness and ability to travel 60–70% with 8–10 DOS per month
Strong organizational, communication, and stakeholder management skills
Work Environment Expectations
Fast-paced, compliance-driven clinical operations setting
Zero tolerance for protocol deviations and timeline delays
Frequently shifting priorities requiring adaptability and proactive decision-making
Team-oriented, collaborative culture
Technology-enabled environment utilizing electronic data capture (EDC) and remote monitoring systems
Compensation and Benefits
Employees working 20 or more hours per week are eligible for comprehensive benefits, including:
Medical, Dental, and Vision Insurance
Life Insurance and Short-Term/Long-Term Disability coverage
401(k) Retirement Plan
Paid Time Off (PTO) – Flex Plan
Employee Recognition Programs
Employee Resource Groups (ERGs)
Work Environment and Physical Requirements
Office-based work with frequent travel to investigative sites (domestic and occasional international travel)
Ability to sit for extended periods and operate a vehicle safely
Repetitive hand and wrist movements for computer and reporting tasks
Occasional bending, stooping, and lifting (15–20 lbs, including luggage and laptop equipment)
Regular and reliable attendance with flexibility for varied working hours
Why Join Fortrea
Fortrea is committed to transforming drug and device development through scientific rigor, operational excellence, and its FOUR values: Forward Together, Own It, Uphold Integrity, and Respect People. As an Ophthalmology CRA II, you will play a critical role in ensuring patient safety and data quality in specialized therapeutic trials that directly impact vision health and quality of life.
Advance your clinical research career in ophthalmology and contribute to global clinical innovation.
Apply now through ThePharmaDaily.com to explore this high-impact opportunity in clinical operations.
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