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Ophthalmology - Cra Ii

Fortrea
Fortrea
1-3 years
preferred by company
10 Dec. 29, 2025
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 (CRA II)

Locations: Multiple Global Locations (Open to Major Hub Cities)
Category: Clinical Research
Job ID: 255475
Employment Type: Full-Time / Remote with Travel


Job Overview

We are seeking an experienced Ophthalmology Clinical Research Associate II (CRA II) to support and lead monitoring activities within a Full-Service Outsourcing (FSO) clinical research model. This role is ideal for CRAs with strong ophthalmology trial experience who thrive in fast-paced, compliance-driven environments and are comfortable with extensive site travel.

The position is open across multiple major hub locations and requires 60–70% travel, averaging 8–10 on-site days per month.


Key Responsibilities

  • Conduct all aspects of clinical site monitoring, including pre-study, initiation, routine monitoring, and close-out visits

  • Ensure effective site management in accordance with project plans, SOPs, ICH-GCP, and regulatory requirements

  • Verify that study staff are adequately trained and equipped to safely enroll and manage trial participants

  • Ensure patient safety and rights, including strict adherence to informed consent processes and protocol compliance

  • Maintain data integrity by performing thorough source data verification (SDV) and CRF review

  • Identify, document, and resolve data discrepancies, missing data, and protocol deviations

  • Manage registry-based studies and conduct feasibility assessments when required

  • Independently handle Serious Adverse Event (SAE) reporting, including narratives and follow-up activities

  • Perform query generation and resolution within sponsor or Fortrea data management systems

  • Support training and mentoring of junior CRAs through co-monitoring and onboarding activities

  • Coordinate assigned clinical projects and, when required, act as a Local Project Coordinator or site-level client contact

  • Collaborate effectively with cross-functional teams, vendors, and site personnel


Required Qualifications

  • Bachelor’s degree or higher in Life Sciences, Nursing, Pharmacy, or a related healthcare discipline

  • Nursing licensure or allied health certification is acceptable

  • Strong understanding of ICH-GCP, regulatory guidelines, and clinical monitoring processes


Experience Requirements

  • 1–3 years of independent clinical monitoring experience

  • Mandatory ophthalmology clinical trial experience

  • Proven ability to manage multiple sites and priorities in a time-sensitive, quality-focused environment


Key Skills & Competencies

  • Strong clinical judgment and attention to detail

  • Excellent communication and interpersonal skills

  • High adaptability to changing priorities and study demands

  • Comfortable working in technology-driven, electronic data capture (EDC) environments

  • Ability to work independently while contributing effectively within cross-functional teams


Work Environment & Travel

  • Remote-based role with frequent domestic travel and occasional international travel

  • Office-based tasks performed in a standard computer and electronic environment

  • Ability to travel extensively and operate a vehicle safely


Physical Requirements

  • Ability to sit for extended periods and perform repetitive hand movements

  • Light to moderate lifting (up to 15–20 lbs), including laptop and travel materials

  • Occasional bending, twisting, crouching, or stooping as required during site visits

  • Flexible availability, including varied working hours as study demands require


Compensation & Benefits

  • Target Salary Range: USD 105,000 – 117,000 (based on title, experience, and location)

  • Comprehensive benefits for eligible employees, including:

    • Medical, Dental, Vision, Life, and Disability Insurance

    • Retirement savings plans (401K)

    • Paid Time Off (PTO) with flexible options

    • Employee recognition programs and resource groups

  • Ongoing professional development and career growth opportunities


Application Information

  • Applications are accepted on an ongoing basis

  • Equal Employment Opportunity and workplace accommodations supported


Why Join This Role

This opportunity allows you to work on specialized ophthalmology clinical trials, partner with global research teams, and contribute directly to advancing treatments that improve patient vision and quality of life worldwide.