Senior Specialist Clinical Trial Transparency
Job Description
Your Role:
Lead and coordinate clinical trial transparency activities across assigned studies and programs, from trial registration through results disclosure and public posting in registries such as ClinicalTrials.gov, the Clinical Trials Information System (CTIS), and local registers. You will manage registry maintenance, review data for completeness and accuracy, and lead document redaction and anonymization for public disclosure in line with regulatory requirements and protection of personal data and commercially confidential information. You will also partner with cross-functional teams to monitor deadlines, maintain compliance, and support audit and inspection readiness. The purpose of this role solves the challenge of complex and evolving global transparency requirements by ensuring accurate, timely, and compliant disclosure practices that strengthen trust in clinical development and support responsible public access to trial information.
Who You Are:
- You bring at least 5 years of experience in clinical research within a contract research organization, study site, pharmaceutical company, or biotechnology company, including strong hands-on experience in clinical trial disclosure and transparency.
- You have solid knowledge of global clinical trial registries, including ClinicalTrials.gov and the Clinical Trials Information System, and understand registration, maintenance, results disclosure, and local registry requirements.
- You are confident working with disclosure systems such as PharmaCM/Disclose or PRIME, and you are comfortable using Microsoft Office 365, Adobe Acrobat and AI in a highly regulated environment.
- You know how to review registry content and disclosure documents for accuracy, consistency, anonymization, and redaction.
- You can interpret and apply global, regional, and local transparency regulations and translate changing requirements into clear operational practice.
- You bring effective spoken and written communication skills and know how to build strong partnerships across multidisciplinary teams and projects.
- You have a degree in life sciences or a healthcare-related discipline and a strong understanding of clinical development, clinical operations, and the broader drug development process.
- You are excited by the opportunity to take end-to-end ownership, contribute to quality and compliance, and make a global impact from Bangalore, India through trial transparency and disclosure excellence.