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Clinical Research Associate

1+ years
Not Disclosed
10 July 30, 2024
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, 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

Company: ICON
Role: Clinical Research Associate (CRA)
Location: Various locations
Position Type: Full-time

About ICON:
At ICON, our people are our greatest asset. Our diverse teams drive us to excel and help us fulfill our mission of advancing and improving patients' lives. Our ‘Own It’ culture is anchored in four core values: Accountability & Delivery, Collaboration, Partnership, and Integrity. We aim to be the leading Clinical Research Organization that delivers excellence in every interaction with clients and patients. If you’re driven by our vision, join us to work in a dynamic, supportive environment with some of the brightest and friendliest professionals in the industry.

Role Overview:
As a Clinical Research Associate at ICON, you'll work within a fast-paced, large-scale environment alongside a dedicated team of CRAs. Your role will involve identifying, selecting, initiating, and closing out investigational sites for clinical studies in phases II – IV, ensuring compliance with applicable regulations and ICH-GCP guidelines. You will coordinate all activities for setting up and monitoring studies, complete accurate status reports, and maintain study documentation.

Key Responsibilities:

  • Independently manage and coordinate all activities related to setting up and monitoring clinical studies.
  • Complete accurate study status reports and maintain detailed study documentation.
  • Efficiently handle sponsor-generated queries and ensure cost efficiency.
  • Participate in preparing and reviewing study documentation and feasibility studies for new proposals as needed.

Qualifications:

  • Minimum of 1 year of experience in onsite monitoring as a CRA.
  • University degree in medicine, science, or a related field.
  • Knowledge of ICH-GCP guidelines and the ability to review and evaluate medical data.
  • Excellent written and verbal communication skills in English.
  • Strong social skills to address queries promptly.
  • Willingness to travel at least 60% of the time (both domestic and international) and possess a valid driver’s license.

Benefits of Working at ICON:

  • Competitive Salary: We offer competitive salary packages, benchmarked against industry standards, with annual bonuses based on performance.
  • Health Benefits: Comprehensive health-related benefits for employees and their families.
  • Retirement Plans: Competitive retirement plans and related benefits such as life assurance.
  • Professional Development: Work in an environment that fosters personal growth and encourages fulfilling your sense of purpose.
  • Inclusive Culture: We are an equal opportunity employer committed to a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment.

Accommodations:
If you need reasonable accommodation for any part of the application process or to perform the essential functions of the position due to a medical condition or disability, please let us know through the provided form.

Current ICON Employees: Click here to apply

Application Process:
Apply online with your current CV/resume and cover letter. ICON is committed to building a diverse team and welcomes all qualified candidates.