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Ophthalmology & Gen Meds - Cra Ii

Fortrea
Fortrea
1-3 years
$105,000–$117,000
Arizona, California, Colorado, United States
10 March 19, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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 & Gen Meds - CRA II

Company: Fortrea
Location: Remote – United States (Multiple Hub Locations: IL, CA, FL, NY, and others)
Job Type: Full-Time | Remote
Experience: Typically 1–3 Years (Clinical Research / Monitoring)
Qualification: University or College Degree, or relevant allied health certification (e.g., nursing licensure)
Salary Range: $105,000–$117,000

Job Overview

Fortrea is hiring an Ophthalmology & General Medicine Clinical Research Associate II (CRA II) to lead and support Full Service Outsourcing clinical trials. The role involves monitoring study sites, ensuring data integrity, protecting participant safety, and coordinating clinical projects. This position requires frequent travel (60–70%, 8–10 days on-site per month) and strong adaptability to fast-paced and technology-driven environments.

Key Responsibilities

Clinical Monitoring & Site Management

Responsible for all aspects of study site monitoring including routine visits, close-outs, and maintenance of study files.
Conduct pre-study and initiation visits and liaise with vendors.
Ensure study staff are trained, and protocol instructions are followed.
Protect study participants by verifying informed consent and adherence to protocol and regulatory requirements.
Monitor Case Report Forms (CRFs) and other data collection tools for accuracy and consistency.
Complete Serious Adverse Event (SAE) reporting, narratives, and follow-up as required.
Undertake registry management and feasibility work as requested.

Data Review & Compliance

Independently perform CRF review, query generation, and resolution per established guidelines.
Ensure integrity and completeness of data collected electronically.
Support training of new employees, including co-monitoring activities.

Project Coordination

Coordinate designated clinical projects as Local Project Coordinator with supervision as needed.
Serve as a local client contact when assigned.
Perform other duties as directed by management.

Required Skills

Clinical & Technical Expertise

1–3 years of clinical monitoring experience.
Knowledge of clinical trial protocols and regulatory requirements.
Ability to work in a fast-paced, technology-driven environment.

Communication & Teamwork

Strong interpersonal and team collaboration skills.
Ability to train and guide site staff and new employees.
Effective problem-solving and organizational skills.

Travel & Flexibility

Comfortable with frequent domestic and occasional international travel.
Adaptable to changing priorities and on-the-spot problem solving.

Basic Qualifications

University or college degree, or certification in a related allied health profession (e.g., nursing licensure).

Preferred Competencies

Experience with electronic data capture (EDC) systems.
Understanding of ophthalmology and general medicine therapeutic areas.
Ability to manage multiple study sites and projects simultaneously.

Key Competencies

Clinical trial site monitoring
Participant safety and informed consent verification
Data review and CRF validation
SAE reporting and follow-up
Project coordination and client liaison
Regulatory compliance and protocol adherence

Work Environment

Office and remote environment with exposure to electrical office equipment.
Frequent travel to client and study sites; occasional international travel.
Physical requirements include extended sitting, repetitive hand movements, bending, lifting (15–20 lbs), and use of computer software.

Benefits

Medical, Dental, Vision, Life, STD/LTD insurance
401(K) plan
Paid time off (PTO) – Flex Plan
Employee recognition awards and resource groups

About the Company

Fortrea partners with leading pharmaceutical, biotechnology, and medical device companies to support clinical research and drug development, focusing on participant safety, data integrity, and operational excellence.