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Clinical Transparency Specialist

Novo Nordisk
Novo Nordisk
10 years
Not Disclosed
Bengaluru, Karnataka, India
10 Feb. 19, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Clinical Transparency Specialist – Clinical Reporting & Disclosure

Company: Novo Nordisk
Department: Clinical Transparency, Clinical Reporting – Global Business Services (GBS)
Location: Bengaluru, Karnataka, India
Employment Type: Full-Time
Application Deadline: 20 February 2026
Industry: Clinical Development & Regulatory Disclosure

Job Overview

Novo Nordisk Global Business Services (GBS) is seeking a highly experienced Clinical Transparency Specialist to join its Clinical Reporting team in Bengaluru. This role is pivotal in ensuring global compliance with clinical trial disclosure requirements, transparency regulations, and data protection standards across international markets.

The selected professional will lead clinical disclosure activities, support regulatory interactions, and drive strategic alignment of clinical reporting processes in accordance with global health authority requirements.

Experience Required

  • Minimum 10 years of experience evaluating and communicating scientific or clinical data, preferably within pharmaceutical companies or CRO environments

  • Strong experience in clinical drug development, GCP compliance, and clinical trial methodology

  • Demonstrated expertise in clinical trial disclosure, transparency regulations, and trial registration processes

  • Experience working in global, project-oriented, cross-functional environments

Educational Qualification

  • PhD or Master’s degree (M.Sc. or equivalent) in Life Sciences or related discipline

Key Responsibilities

 Perform clinical disclosure and transparency activities including trial registration, results posting,   and audit readiness.

  • Ensure compliance with global regulatory requirements governing clinical trial disclosure.

  • Act as the primary point of contact for stakeholders regarding Clinical Reporting-related documentation.

  • Lead strategic discussions and align project strategies with Clinical Reporting objectives.

  • Drive updates to templates, SOPs, and disclosure-related documentation processes.

  • Represent Clinical Reporting in global project teams and regulatory interactions.

  • Implement data protection measures such as redaction and anonymization prior to public disclosure.

  • Support submissions to regulatory authorities and clinical trial registries.

  • Drive process optimization, digital innovation, and continuous improvement initiatives within disclosure operations.

Regulatory & Authority Exposure

The role supports transparency submissions and documentation compliance for global health authorities, including:

  • European Medicines Agency (EMA)

  • Health Canada

  • Global clinical trial registries and international regulatory bodies

Required Skills & Competencies

  • Deep understanding of global clinical trial disclosure regulations

  • Strong knowledge of ICH-GCP guidelines and clinical reporting standards

  • Experience with disclosure and transparency IT systems

  • Excellent stakeholder management and communication skills

  • Strategic thinking and decision-making capabilities

  • Ability to manage multiple global projects with high attention to detail

  • Strong quality mindset with inspection-readiness approach

About the Department

The Clinical Reporting team in Bengaluru serves as Novo Nordisk’s Centre of Excellence for Clinical Transparency and Results Disclosure. Since its establishment in 2014, the unit has expanded to manage global transparency obligations, ensuring clinical trial documents such as protocols, reports, and synopses are disclosed responsibly and compliantly.

The team plays a critical role in safeguarding patient data privacy while maintaining scientific transparency for regulators, researchers, and the public.

Why Join Novo Nordisk?

With more than a century of innovation in chronic disease management, Novo Nordisk remains committed to advancing patient safety and transparency in drug development. Employees benefit from global exposure, structured quality frameworks, and the opportunity to contribute to international clinical compliance initiatives.

Important Information

Novo Nordisk does not charge recruitment fees and does not extend unsolicited employment offers. Applicants are encouraged to verify official communication channels before sharing personal information.

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