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Clinical Research Associate 1, 2 / Sr. Cra 1 - Ophthalmology & Biopharma - West Coast

3+ years
$100-140K
10 Jan. 18, 2025
Job Description
Job Type: Full Time 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

Position: Clinical Research Associate 1, 2 / Sr. CRA 1 - Ophthalmology & Biopharma (West Coast)
Location: Remote (United States)
Category: Clinical
Job ID: 2444246


Job Overview

Fortrea is actively seeking Clinical Research Associates (CRA 1, 2, and Sr. CRA 1) for Full-Service Outsourcing in General Medicine therapeutic areas, with a preference for those located in West Coast hub areas. In this role, you will leverage your clinical skills and judgment to provide high-standard care for participants in clinical trials. You will also respond to emergency situations based on clinical research standards and manage study site monitoring and data integrity.

Key Responsibilities

  • Site Management & Monitoring:
    • Conduct routine site monitoring, site close-out, and study file maintenance.
    • Perform pre-study and initiation visits, liaising with vendors and managing study staff to ensure proper protocol adherence.
    • Ensure patient safety and adherence to informed consent procedures and regulatory guidelines.
  • Data Integrity & Reporting:
    • Monitor the integrity of data on Case Report Forms (CRFs) and other data collection tools.
    • Perform Serious Adverse Event (SAE) reporting and follow-up.
    • Assist with CRF review, query generation, and resolution in client data management systems.
  • Training & Coordination:
    • Assist in training new employees and co-monitoring tasks.
    • Act as a Local Project Coordinator and communicate with clients as assigned.
  • Other Duties:
    • Participate in feasibility studies and perform other duties as required by management.

Qualifications

  • Education:
    • University or college degree or certification in a related health profession (e.g., nursing licensure).
  • Experience:
    • 6 months to 3+ years of Clinical Monitoring experience.
    • Ophthalmology experience is preferred, but not required.
    • Ability to work in a fast-paced, technology-driven environment with shifting priorities.
  • Skills:
    • Strong teamwork and communication skills to ensure smooth study operations.
    • Comfort working in an environment that emphasizes data integrity and protocol adherence.

Compensation & Benefits

  • Pay Range: $100,000 - $140,000 (based on title)
  • Benefits:
    • Comprehensive benefits including medical, dental, vision, life, STD/LTD, 401(K), PTO (flex plan), employee recognition awards, and multiple employee resource groups (ERGs).

Company Overview

Fortrea is a global leader in clinical research, revolutionizing the development process to deliver life-changing therapies and solutions to patients worldwide.

Equal Opportunity Employer Statement

Fortrea is committed to diversity and inclusion in the workforce and does not tolerate any form of discrimination or harassment. Employment decisions are made based on qualifications and business needs.

Accommodation

For accommodations during the hiring process, please contact taaccommodationsrequest@fortrea.com.