Senior Cra- Texas

2+ years

Not Disclosed

United States

10 April 18, 2025

Job Description

Job Type: Full Time Remote 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

Job Title:

Senior Clinical Research Associate (CRA)

Location:

Texas, United States (Remote)

Job ID:

2025-117740

Department:

Clinical Monitoring – ICON Strategic Solutions

Job Type:

Full-Time, Remote

Application Contact:

Name: Melissa Benner
Options: View other roles or send a direct message through the platform

Job Description:

As a Senior CRA, you will ensure the smooth progression of clinical trials by monitoring investigative sites or remotely, ensuring compliance with protocols, SOPs, ICH-GCP, and all applicable regulatory requirements. You will be responsible for the safety of trial subjects and the integrity of clinical data, providing mentorship to new CRAs and conducting site evaluations.

Key Responsibilities:

Apply knowledge of ICON’s policies and procedures for monitoring clinical trials
Monitor trials for subject safety and data integrity
Conduct monitoring visits and ensure compliance with ICH-GCP and SOPs
Manage investigative sites and facilitate trial deliverables
Identify scientific misconduct and escalate issues when necessary
Mentor new CRAs and serve as an observation visit leader
Assist with the development of trial tools and documents
Participate in process improvements and training of trial teams

Requirements:

Education:
- Undergraduate degree in clinical, science, or health-related field
- Health care professional licensure (e.g., Registered Nurse) or equivalent experience
Experience:
- 2+ years of experience supporting clinical trials with 1 year of on-site monitoring (CRA2) or 4+ years with 3 years of on-site monitoring (CRA3)
- Proficiency with Microsoft Office and clinical systems
- Experience in monitoring all trial components (PSSV to COV) is preferred
- Ability to travel for approximately 10 site visits per month

Benefits:

Competitive salary and annual leave
Health insurance options for you and your family
Retirement planning with strong savings benefits
Global Employee Assistance Program (TELUS Health)
Life assurance
Country-specific optional benefits (childcare vouchers, gym memberships, etc.)
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Inclusion & Accessibility:

ICON is committed to an inclusive and accessible environment for all candidates, ensuring equal consideration for employment.
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Senior Cra- Texas

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