Clinical Transparency Specialist – Clinical Development
Location: Bangalore, Karnataka, India
Department: Clinical Transparency, Clinical Reporting
Company: Novo Nordisk
Application Deadline: 20 February 2026
Overview
The Clinical Transparency Specialist plays a critical role in ensuring global clinical trial disclosure, regulatory transparency, and compliance with international health authority requirements. This position is based at the Novo Nordisk Global Business Services (GBS) center in Bangalore and supports global Clinical Reporting initiatives aligned with regulatory standards and data protection frameworks.
This role is ideal for senior clinical development professionals with deep expertise in clinical trial disclosure, audit readiness, regulatory documentation, and global transparency requirements.
Key Responsibilities
Execute end-to-end clinical disclosure and transparency activities, including trial registration, results posting, and regulatory submissions.
Ensure audit readiness and manage health authority interactions related to disclosure requirements.
Serve as the primary point of contact for stakeholders on Clinical Reporting-driven documents and content.
Drive strategic discussions and ensure alignment between Clinical Reporting objectives and project strategies.
Lead cross-functional meetings and prioritize disclosure deliverables across global projects.
Contribute to the development and continuous improvement of templates, SOPs, and governance frameworks.
Implement process enhancements, digital innovations, and efficiency initiatives within transparency operations.
Represent Clinical Reporting in global project teams to ensure compliance with international regulatory frameworks.
Apply data protection measures such as redaction and anonymization before public or regulatory release of clinical documents.
Required Qualifications
PhD or Master’s degree (M.Sc. or equivalent) in Life Sciences, Pharmacy, Medicine, or related field.
Minimum 10 years of experience in evaluating and communicating clinical data, preferably within pharmaceutical or CRO environments.
Strong knowledge of global regulatory requirements for clinical trial disclosure and transparency.
Hands-on experience in clinical drug development, GCP (Good Clinical Practice), clinical trial methodology, and trial registration processes.
Experience working in international, cross-functional, project-driven organizations.
Proficiency in IT systems and digital platforms supporting clinical disclosure and transparency workflows.
About the Clinical Transparency Team
The Bangalore-based Clinical Reporting team functions as a global Centre of Excellence for Results Disclosure. Established in 2014, the unit supports worldwide transparency requirements by preparing and managing key clinical trial documents, including:
Clinical trial protocols
Clinical Study Reports (CSRs)
Synopses and disclosure documents
The team ensures compliance with regulatory bodies such as the European Medicines Agency and Health Canada, along with global clinical trial registries. All disclosures are conducted in accordance with data protection regulations and internal compliance standards.
Why Join Novo Nordisk?
With over 100 years of scientific innovation, Novo Nordisk is committed to advancing long-term healthcare solutions for chronic diseases. The organization fosters a collaborative, inclusive, and purpose-driven work environment where clinical excellence and regulatory integrity are central to patient trust and global impact.
Application Process
Interested candidates should apply online by submitting an updated CV before 20 February 2026.
Novo Nordisk follows a transparent recruitment process and does not request fees, payments, or purchases at any stage of hiring. Applicants are advised to be cautious of fraudulent recruitment communications.
Equal Opportunity Statement
Novo Nordisk is committed to an inclusive recruitment process and equal opportunity for all applicants, supporting diversity across global teams.
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