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Senior Clinical Research Associate- Ca

4+ years
$110,520.00 – $138,150.00 USD
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 – CA


Location:

United States (Remote, California preferred)


Job ID:

2025-117080


Department:

Clinical Monitoring (ICON Strategic Solutions)


Job Type:

Full-Time, Remote


Application Contact:

Name: Melissa Benner
Message Option: Available through job platform
View Roles: See other roles managed by Melissa


Job Description:

About ICON:
ICON plc is the world’s largest and most comprehensive clinical research organization, powered by healthcare intelligence. This role supports ICON’s mission of transforming clinical development by delivering high-quality data and operational excellence.


Key Responsibilities:

  • Conduct site evaluation, initiation, interim monitoring, and close-out visits.

  • Evaluate site feasibility and staff availability for study execution.

  • Ensure compliance with ICH-GCP, study protocols, and regulatory requirements.

  • Build and maintain strong relationships with clinical sites and investigators.

  • Oversee site-level execution of clinical studies, including risk identification and mitigation.

  • Monitor subject safety data including AEs/SAEs, and ensure proper documentation.

  • Perform source data verification (SDV) and ensure data entered in CRFs matches medical records.

  • Track and report on progress and escalate issues as necessary.

  • Ensure timely and compliant completion of monitoring visit reports and updates to databases (e.g., Veeva, eTrack).

  • Coordinate supply delivery and accountability at clinical sites.

  • Ensure inspection-readiness of site and sponsor records.


Qualifications & Experience:

  • Education:

    • Bachelor’s degree in life sciences or health-related field

    • Licensed healthcare professional (e.g., RN) or equivalent work experience preferred

  • Experience:

    • Minimum 4+ years of clinical monitoring experience

    • Experience in monitoring all trial components (PSSV to COV)

    • Prior mentoring/coaching of junior CRAs is a plus

  • Skills:

    • Strong written and verbal communication in English and local language

    • Excellent organizational and multitasking abilities

    • Working knowledge of ICH-GCP and local regulations

    • Travel availability required

    • Familiarity with electronic systems like Veeva Vault, RAMOS, eTrack


Salary Range:

$110,520.00 – $138,150.00 USD
(Compensation varies based on location, experience, education, and skill set)


ICON Employee Benefits Include:

  • Generous annual leave policies

  • Health insurance for employees and dependents

  • Competitive retirement plans

  • Global Employee Assistance Program (TELUS Health) – 24/7 access

  • Life assurance

  • Flexible country-specific perks:

    • Childcare vouchers

    • Bike-to-work schemes

    • Gym discounts

    • Subsidized travel passes

    • Health screenings

More details: ICON Benefits Page


Diversity & Inclusion:

ICON supports equal opportunity and a culture of inclusion. No candidate is discriminated against based on race, gender, orientation, disability, or veteran status.

Reasonable accommodations info:
Request Accommodations