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Ophthalmology Cra Ii & Sr. Cras

1-3 years
$105,000 – $140,000
10 Oct. 4, 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

🧠 Position Title:

Ophthalmology CRA II & Sr. CRAs


🌍 Locations:

Available in 14 locations across the U.S.
(Open to major hub locations across the U.S.)


🧩 Category:

Clinical


🆔 Job ID:

254315


🏢 Job Type:

Full Service Outsourcing Team
(#LI - Remote)


🎯 Job Overview:

We are seeking experienced Ophthalmology Clinical Research Associates (CRAs) to lead and support our Full Service Outsourcing team. You will leverage your clinical skills, knowledge, and judgment to ensure a high standard of care for participants in clinical trials, while maintaining regulatory compliance and data integrity.


💼 Key Responsibilities:

🔹 Site Monitoring & Management

  • Conduct routine monitoring, pre-study, initiation, and close-out visits.

  • Maintain study files and liaise with vendors as required.

  • Ensure site management activities are performed according to project plans.

🔹 On-Site Responsibilities

  • Confirm that study staff are properly trained and equipped to safely enroll participants.

  • Protect patient safety by verifying informed consent procedures and protocol adherence.

  • Ensure data integrity through careful source document verification (SDV).

  • Identify and resolve missing or implausible data in CRFs or other data collection tools.

🔹 Regulatory & Quality

  • Manage registry activities as outlined in project plans.

  • Conduct feasibility assessments when required.

  • Handle Serious Adverse Event (SAE) reporting, documentation, and follow-up.

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

  • Maintain compliance with Fortrea or client data management systems.

🔹 Team Support & Coordination

  • Support training and mentoring of new CRAs (e.g., co-monitoring).

  • Serve as a Local Project Coordinator (LPC), and act as a local client contact when assigned.

  • Perform other tasks as assigned by management.


🎓 Requirements:

  • Education:

    • Bachelor’s degree or equivalent in Life Sciences or related allied health profession (e.g., nursing licensure).

  • Experience:

    • 1 – 3+ years of Clinical Monitoring experience.

    • Ophthalmology experience strongly preferred.

  • Technical & Soft Skills:

    • Comfortable in fast-paced, tech-based environments.

    • Strong attention to detail; no protocol deviations tolerated.

    • Ability to prioritize under changing conditions.

    • Excellent teamwork and communication skills.


⚙️ Work Environment:

  • Fast-paced: Strict adherence to timelines and protocols.

  • Dynamic: Frequent changes in priorities; adaptability required.

  • Collaborative: Strong teamwork needed for trial success.

  • Digital-first: All data collected and managed in electronic systems.


💰 Compensation & Benefits:

Target Pay Range (Based on Title):
💵 $105,000 – $140,000 (Annual)

Eligible Employees (20+ hours/week) Receive:

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

  • 💼 401(k) Retirement Plan

  • 🌴 Paid Time Off (PTO) – Flex Plan

  • 🏆 Employee Recognition Awards

  • 🌐 Employee Resource Groups (ERGs)


📅 Application Details:

Applications accepted on an ongoing basis.


⚖️ EEO & Accommodations:

Learn more about our Equal Employment Opportunity (EEO) and Accommodations policy [here].