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Ophthalmology Cra Ii & Sr. Cras

1-3 years
$105,000 – $140,000
10 Sept. 30, 2025
Job Description
Job Type: Full Time 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. CRAs

Locations: 14 Locations (US – major hub locations)
Category: Clinical
Job ID: 254315


Job Summary:

The Ophthalmology CRA II & Sr. CRAs are responsible for site monitoring and management within ophthalmology clinical trials. The role ensures patient safety, data integrity, and compliance with study protocols, and may include acting as Local Project Coordinator and supporting new employee training.


Key Responsibilities:

1. Site Monitoring & Management:

  • Conduct all aspects of study site monitoring, including routine monitoring and site close-out.

  • Maintain study files, conduct pre-study and initiation visits, and liaise with vendors.

  • Perform all aspects of site management as defined in project plans.

  • Undertake feasibility work as requested.

2. On-Site Monitoring:

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

  • Verify informed consent procedures and adherence to protocol requirements to protect study participants.

  • Review source documents to ensure data integrity on CRFs or other collection tools.

  • Monitor for missing or implausible data.

3. Registry & SAE Management:

  • Responsible for registry management as prescribed in project plans.

  • Complete Serious Adverse Event (SAE) reporting, including report production, narratives, and follow-up.

  • Independently perform CRF review, query generation, and resolution per established data review guidelines.

4. Mentoring & Project Coordination:

  • Assist with training new employees through co-monitoring.

  • Coordinate designated clinical projects as Local Project Coordinator (with supervision if applicable).

  • May act as local client contact as assigned.

5. Additional Responsibilities:

  • Perform other duties as assigned by management.


Requirements:

Education:

  • University or college degree, or certification in a related allied health profession (e.g., nursing licensure) from an accredited institution.

Experience:

  • 1–3+ years of Clinical Monitoring experience.

  • Ophthalmology experience preferred.

Skills & Competencies:

  • Comfortable working in a fast-paced environment with strict protocol adherence.

  • Adaptable to changing priorities.

  • Strong teamwork and interpersonal skills.

  • Proficient with electronic data collection and technology-based workflows.


Compensation & Benefits:

  • Target Pay Range: $105,000 – $140,000

  • Eligible for comprehensive benefits including:

    • Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)

    • 401(K)

    • Paid Time Off (PTO) – Flex Plan

    • Employee recognition awards

    • Employee Resource Groups (ERGs)


Work Environment:

  • #LI - Remote

  • Fast-paced, technology-driven, team-oriented environment.


Additional Information: