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Clinical Trial Assistant

6 months years
Not Disclosed
10 Dec. 6, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

The Clinical Trial Assistant role at ICON is based in Chennai and involves providing administrative and operational support to the Clinical Trial Management and Project Management teams. This role is key in ensuring efficient project tracking and supporting inspection readiness.

Key Responsibilities:

  1. Administrative Support: Assist Project Managers and Clinical Trial Managers with operational activities.

  2. Documentation and Tracking: Maintain and track clinical study documentation, ensuring accurate and up-to-date records.

  3. Study Coordination: Coordinate study materials and collate relevant study information.

Qualifications:

  • Education: Ideally, a degree in Life Sciences.

  • Experience: A minimum of 6 months of experience in Clinical Research.

  • Skills:

    • Strong organizational and administrative abilities.

    • Excellent written and verbal communication skills.

    • Working knowledge of Microsoft Word, Excel, Outlook, and PowerPoint.

Benefits:

  • Competitive salary and a wide range of benefits, including health insurance, life assurance, and retirement planning.

  • Employee Assistance Program for well-being support.

  • Flexible country-specific optional benefits, including childcare vouchers, gym memberships, and more.

ICON fosters a diverse, inclusive, and harassment-free environment, encouraging applicants from all backgrounds.