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Ophthalmology Cra Ii & Sr. Cras

1-3 years
Not Disclosed
10 Oct. 6, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Job Title:

Ophthalmology CRA II & Sr. CRA

Locations:
14 major hub locations across the US

Category: Clinical
Job ID: 254315
Target Pay Range: $105K–$140K
Work Mode: Remote (#LI - Remote)


Job Overview

The Ophthalmology CRA II & Sr. CRA will lead and support the Full Service Outsourcing (FSP) team, ensuring high standards of clinical care for trial participants and responding to emergency situations in accordance with clinical research standards.


Primary Responsibilities

Site Monitoring & Management:

  • Conduct routine and close-out monitoring of clinical sites.

  • Maintain study files and conduct pre-study and initiation visits.

  • Liaise with vendors as required.

  • Manage all aspects of site management as outlined in project plans.

  • Perform feasibility assessments when requested.

General On-Site Monitoring:

  • Ensure study staff have proper materials and instructions to safely enroll participants.

  • Verify adherence to informed consent procedures and protocol requirements.

  • Ensure integrity of data submitted on CRFs or other data collection tools.

  • Monitor data for missing, incomplete, or implausible entries.

  • Manage all aspects of registry administration.

Safety & Data Management:

  • Complete SAE reporting, generate narratives, and perform follow-up.

  • Independently perform CRF review, query generation, and resolution using established guidelines on Fortrea or client data management systems.

Team Support & Coordination:

  • Assist in training new employees (e.g., co-monitoring).

  • Coordinate designated clinical projects as a Local Project Coordinator, acting as local client contact if applicable.

  • Perform other duties as assigned by management.


Qualifications / Skills

Minimum Required:

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

  • 1–3+ years of clinical monitoring experience.

  • Strong teamwork and communication skills.

  • Comfortable working in a fast-paced, technology-driven, and dynamic environment.

Preferred:

  • Ophthalmology clinical trial experience.

  • Experience in electronic data capture environments.


Work Environment & Culture

  • Fast-paced with strict adherence to study protocols and timelines.

  • Frequently changing priorities requiring adaptability.

  • Technology-focused environment for direct electronic data capture.

  • Emphasis on teamwork and collaboration.


Benefits

  • Comprehensive benefits for regular full-time or part-time employees (20+ hours/week) including:

    • Medical, Dental, Vision, Life, STD/LTD insurance

    • 401(K) plan

    • Paid Time Off (PTO) – Flex Plan

    • Employee recognition awards

    • Multiple Employee Resource Groups (ERGs)