Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

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