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Senior Clinical Trial Transparency Associate

5+ years
Not Disclosed
10 June 4, 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

 

Senior Clinical Trial Transparency Associate

Location: India
Job ID: 2025-118314
Company: ICON Strategic Solutions (Other Office Based)


About the Role

Join the world’s largest and most comprehensive clinical research organization as a Senior Clinical Transparency Lead. You will oversee clinical trial registration, disclosure of results, and public disclosure strategies, ensuring compliance with global transparency standards and timely reporting.

Key Responsibilities:

  • Assess and prioritize clinical trial registration and disclosure requirements

  • Oversee daily Clinical Transparency or Public Disclosure operations, ensuring timely review, updates, and approval of registrations and results disclosures

  • Manage review and approval processes and coordinate communications with partners and collaborators

  • Conduct periodic reviews of active registrations and update disclosure strategy plans

  • Use independent judgment to resolve issues and escalate when necessary

  • Coordinate and supervise consultants and vendors involved in transparency activities

  • Address inquiries and provide feedback to leadership on evolving transparency requirements

  • Lead retrospective compliance reviews in response to new regulations

  • Develop training materials and educate teams on transparency policies and procedures

  • Establish global working relationships and communicate changes across the organization

  • Drive process improvements and evaluate automation tools for efficiency

  • Lead training sessions for global colleagues on clinical trial transparency


Qualifications and Experience:

  • Bachelor’s Degree or equivalent experience required

  • Minimum 5 years pharmaceutical industry experience, with a focus on Transparency and/or Disclosure activities

  • Working knowledge of clinical drug development and clinical trial protocols

  • Excellent organizational skills and high attention to detail

  • Self-directed and motivated, able to work independently

  • Proficient with MS Word and Excel

  • Healthcare professional background preferred


What ICON Offers:

  • Competitive salary and benefits package including health insurance, retirement planning, and life assurance

  • Global Employee Assistance Program for well-being support

  • Flexible benefits tailored to country-specific needs (childcare vouchers, gym memberships, travel passes, etc.)

  • Inclusive and accessible workplace culture