Ophthalmology - Cra Ii

Fortrea

1-3 years

preferred by company

Remote

10 Jan. 6, 2026

Job Description

Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Ophthalmology Clinical Research Associate II (CRA II) – Remote, USA
Locations: Multiple hub locations across East & West Coast, USA
Job Type: Full-Time, Remote with 60–70% Travel (8–10 DOS per month)
Experience Required: 1–3 years in Clinical Monitoring, Ophthalmology experience required

About Fortrea
Fortrea is a leading full-service outsourcing Clinical Research Organization (CRO), supporting innovative clinical trials across therapeutic areas, including ophthalmology. We partner with top pharmaceutical, biotechnology, and medical device companies to advance novel therapies and deliver high-quality clinical trial outcomes.

Role Overview
We are seeking an experienced Ophthalmology CRA II to join our Full-Service Outsourcing team. This role combines clinical expertise, project coordination, and regulatory compliance to ensure the successful execution of ophthalmology clinical trials. The ideal candidate thrives in a fast-paced, technology-driven environment and is comfortable managing multiple sites while maintaining strict adherence to protocols.

Key Responsibilities

Lead and perform all aspects of study site monitoring, including initiation, routine visits, and close-out activities.
Ensure protocol compliance, patient safety, and regulatory adherence, including verification of informed consent and adherence to Good Clinical Practice (GCP).
Maintain accurate and comprehensive study documentation, including Case Report Forms (CRFs), study files, and registry management.
Monitor data integrity, identify missing or implausible data, and independently generate and resolve queries.
Conduct Serious Adverse Event (SAE) reporting, including production of narratives and follow-up.
Provide co-monitoring and training support for new employees and act as a local project coordinator or client contact, as needed.
Undertake feasibility assessments and assist in study planning and execution.
Collaborate with cross-functional teams and vendors to ensure timely project delivery.
Perform additional responsibilities as assigned by management.

Qualifications & Experience

University or college degree, or certification in a related allied health profession (e.g., nursing license).
1–3 years of clinical monitoring experience in ophthalmology clinical trials.
Strong knowledge of GCP, regulatory requirements, and clinical trial processes.
Comfortable with remote work, frequent travel, and flexible scheduling.
Strong communication, organizational, and teamwork skills.
Technologically proficient; experience with electronic data capture systems is preferred.

Work Environment & Physical Requirements

Office-based work with exposure to electrical office equipment.
Frequent domestic and occasional international travel to clinical sites.
Ability to sit for extended periods and safely operate a vehicle.
Repetitive hand movements, occasional crouching, stooping, bending, and twisting.
Light to moderate lifting of objects up to 15–20 lbs.
Ability to maintain consistent attendance and adapt to variable hours.

Compensation & Benefits

Target salary range: $105,000–$117,000 annually
Comprehensive benefits package including:
- Medical, Dental, Vision, Life, STD/LTD insurance
- 401(k) retirement plan
- Paid time off (PTO) – Flex Plan
- Employee recognition programs and multiple ERGs (Employee Resource Groups)

Why Join Fortrea?

Work in a fast-paced, high-impact environment where patient safety and protocol compliance are paramount.
Collaborate with cross-functional teams on innovative ophthalmology clinical trials.
Opportunity to gain extensive travel experience and professional growth in clinical research.
Contribute to data-driven, high-quality clinical research that advances patient care.

EEO & Accommodations
Fortrea is an Equal Opportunity Employer. We are committed to creating an inclusive workplace and providing reasonable accommodations throughout the recruitment and employment process.

Apply Now
If you are an experienced Ophthalmology CRA II seeking a challenging and rewarding clinical research role, apply today to join Fortrea’s global team and drive excellence in clinical trial execution.

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Ophthalmology - Cra Ii

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