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Clinical Scientific Expert - I

5-7 years
Not Disclosed
10 Sept. 11, 2025
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

Company: Novartis Healthcare Private Limited
Division: Development
Business Unit: Innovative Medicines
Location: Hyderabad, India
Employment Type: Regular (Full-time)
Functional Area: Research & Development
Shift Work: No


About the Role

As a Clinical Scientific Expert I, you will be responsible for supporting the execution of clinical trials and related activities, ensuring quality, compliance, and operational excellence. This role involves collaboration across multiple functions to drive impactful outcomes for patients.


Major Accountabilities

  • Implement issue resolution plans for assigned studies/programs.

  • Assist with program-level activities, including tracking and reporting.

  • Manage interactions with cross-functional teams such as:

    • Data Management

    • Drug Supply Management

    • Clinical Development

    • Novartis Country Pharma Organizations

  • Report technical complaints, adverse events, and special case scenarios related to Novartis products within 24 hours of receipt.

  • Support distribution of marketing samples (where applicable).


Key Performance Indicators (KPIs)

  • Timely, efficient, and quality execution of assigned trials and activities within budget and compliance standards.

  • Proactive operational planning with effective risk mitigation and contingency strategies.

  • For Clinical Scientific Expert I specifically:

    • Perform clinical data review and provide insights with accuracy, consistency, and inspection readiness.

    • Deliver high-quality contributions to study documents (e.g., protocol, informed consent forms, clinical sections of CTAs).

  • Demonstrate Novartis Values & Behaviors: Innovation, Quality, Collaboration, Performance, Courage, and Integrity.


Minimum Requirements

Work Experience

  • Proven experience in:

    • Cross-cultural collaboration

    • Operations management and execution

    • Project management

    • Working across organizational boundaries

Skills

  • Clinical research and trial protocols

  • Clinical trial execution and monitoring

  • Data integrity and risk monitoring

  • Learning design and trend analysis

  • Strong life sciences background

Languages

  • Proficiency in English (written and spoken)


Why Novartis

Helping people with diseases and their families takes more than innovative science—it requires collaboration, support, and inspiration. At Novartis, you’ll work with passionate colleagues to achieve breakthroughs that change patients’ lives.

Learn more: Novartis People & Culture


Benefits and Rewards

Explore our comprehensive benefits designed to help you thrive both personally and professionally:
Novartis Benefits & Rewards Handbook


Join Our Network

Not the right role? Stay connected with Novartis to learn about future opportunities:
Join the Novartis Talent Network


Accessibility and Accommodation

Novartis is committed to providing reasonable accommodation to individuals with disabilities. If you need support during the recruitment process or to perform job functions, please contact:
📩 diversityandincl.india@novartis.com (include job requisition number in your request).


Inclusion Commitment

We are dedicated to building an outstanding, inclusive work environment and fostering diverse teams that represent the patients and communities we serve.