Job Title: Associate Director – Clinical Data Management
Company: Novo Nordisk
Location: Bangalore, Karnataka, India
Employment Type: Full-time
Department: Clinical Data Management & Programming (CDMP), Research & Development
Work Mode: Hybrid (3 days/week in office)
Experience Required: 10+ years in Clinical Data Management/Drug Development with at least 3 years of people leadership or project management experience in the pharmaceutical industry.
Education: Bachelor's or Master's degree in Life Sciences, Pharmacy, Biotechnology, or a related field, with leadership training preferred.
Salary Package: ₹45–70 LPA (Estimated as per current market standards for Associate Director roles in global pharmaceutical companies; final compensation depends on experience, leadership expertise, and interview performance.)
Key Responsibilities:
Lead and implement Clinical Data Management & Programming (CDMP) strategies across therapeutic areas.
Drive high-quality clinical data deliverables while ensuring regulatory and GCP compliance.
Provide tactical leadership for department strategy, operations, and people management.
Lead hiring, coaching, mentoring, performance management, and workforce planning.
Collaborate with Clinical Pharmacology, Biostatistics, Clinical Operations, Trial Operations, and Clinical Reporting teams.
Support Clinical Pharmacology, Phase I, NIS, and DAS clinical trial activities.
Manage departmental budgets, resource allocation, and project planning.
Drive process improvements, innovation, and adoption of new clinical data science methodologies.
Ensure compliance with GxP, regulatory guidelines, and company quality standards.
Influence clinical development decisions through data management expertise and cross-functional collaboration.
Required Skills:
Clinical Data Management (CDM)
Clinical Data Programming (CDMP)
Drug Development
Clinical Trial Operations
GCP & GxP Compliance
Regulatory Submissions
Clinical Pharmacology
Project & Portfolio Management
People Leadership
Resource & Budget Management
Stakeholder Management
Process Improvement
Risk Management
Strategic Planning
Change Management
Cross-functional Collaboration
Communication & Negotiation Skills
Preferred Skills:
Experience in global pharmaceutical organizations.
Leadership experience managing international teams.
Knowledge of Phase I, NIS, and DAS studies.
Experience with regulatory authority submissions.
Strong understanding of clinical development lifecycle and data governance.
Benefits:
Competitive leadership compensation package.
Hybrid working model with flexibility.
Career growth and leadership development opportunities.
Exposure to global clinical development programs.
Collaborative and innovation-driven work environment.
Opportunity to lead strategic initiatives at one of the world's leading pharmaceutical companies.
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