Clinical Transparency Specialist
Category: Clinical Development
Function: Clinical Reporting & Clinical Transparency
Location: Bangalore, Karnataka, India
Organization: Novo Nordisk Global Business Services (GBS)
Application Deadline: February 20, 2026
About Novo Nordisk
Novo Nordisk is a global healthcare company with more than a century of innovation focused on defeating serious chronic diseases. With a strong commitment to scientific integrity, transparency, and patient safety, Novo Nordisk operates across international markets through collaborative, purpose-driven teams. The Global Business Services (GBS) center in Bangalore plays a critical role in supporting global clinical development, regulatory compliance, and transparency initiatives.
Position Overview
The Clinical Transparency Specialist will be responsible for driving end-to-end clinical disclosure and transparency activities in alignment with global regulatory requirements. This role supports Novo Nordisk’s commitment to responsible data sharing, audit readiness, and high-quality clinical reporting. The position requires strong regulatory knowledge, leadership capabilities, and experience working within global, cross-functional clinical development environments.
Key Responsibilities
Execute clinical disclosure and transparency activities, including trial registration, results disclosure, audit readiness, and health authority interactions
Own and manage clinical disclosure deliverables, ensuring compliance with global regulatory standards and internal policies
Contribute to the development, maintenance, and updates of disclosure-related templates, SOPs, and guidance documents
Act as the primary point of contact for stakeholders on Clinical Reporting-driven documentation and transparency content
Lead discussions, align disclosure strategies, and ensure decisions support overall Clinical Reporting and project objectives
Plan, prioritize, and lead meetings to integrate Clinical Reporting strategies into global project plans
Represent Clinical Reporting in cross-functional and project governance forums
Drive continuous improvement initiatives, process optimization, and digital innovation while maintaining a strong quality mindset
Promote knowledge sharing, capability building, and collaboration across global stakeholders
Ensure global regulatory compliance with clinical transparency requirements across regions, including trial registries and health authorities
Required Qualifications and Experience
Education:
PhD or Master’s degree (M.Sc. or equivalent) in Life Sciences or a related scientific discipline
Experience:
Minimum 10 years of relevant experience in data evaluation, scientific communication, or clinical reporting within the pharmaceutical or CRO environment
Core Competencies and Expertise:
In-depth knowledge of global regulatory requirements for clinical trial disclosure and transparency
Strong experience in clinical drug development, Good Clinical Practice (GCP), and clinical trial methodology
Proven expertise in clinical trial registration, results disclosure, and health authority submissions
Experience working in complex, global, project-based organizations
Familiarity with IT systems and digital tools supporting disclosure and transparency processes
Strong stakeholder management, communication, and leadership skills
About the Department
You will join the Clinical Reporting team within Novo Nordisk GBS Bangalore, a center of excellence for clinical disclosure and transparency established in 2014. The team consists of highly experienced Clinical Disclosure Professionals supporting Novo Nordisk’s global transparency commitments.
The department ensures that clinical trial protocols, clinical study reports, synopses, and related documents are prepared and disclosed in compliance with regulatory requirements, data privacy laws, and internal standards. Activities include anonymization, redaction, and disclosure of clinical documents to regulatory authorities, researchers, and public platforms, including submissions to agencies such as the European Medicines Agency (EMA), Health Canada, and global clinical trial registries.
Working at Novo Nordisk
Novo Nordisk fosters a culture of curiosity, collaboration, and accountability. Employees are empowered to challenge conventions, innovate responsibly, and contribute to long-term improvements in global health. The organization values diversity, inclusion, and ethical conduct, offering a professional environment where individuals can grow while making a meaningful impact.
Recruitment Integrity and Equal Opportunity
Novo Nordisk is committed to an inclusive and equitable recruitment process and provides equal employment opportunities to all applicants. The company does not request fees, personal financial information, or equipment purchases as part of the recruitment process. Candidates are encouraged to remain vigilant against fraudulent job offers.
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