Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Clinical Scientific Expert - I

Novartis
Novartis
0-2 years
Not Disclosed
10 Dec. 29, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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 Scientific Expert I
Job ID: REQ-10060761
Location: Hyderabad, India
Employment Type: Full-Time, Regular

Company Overview:
Novartis Healthcare Private Limited is dedicated to transforming lives through innovative therapies and patient-focused clinical research. As part of our commitment to scientific excellence, we are seeking a highly motivated Clinical Scientific Expert I to join our global clinical trial team in India.

Position Summary:
The Clinical Scientific Expert I (CSE I) provides comprehensive clinical and scientific support across all phases of clinical studies under the guidance of the (A)CD(M)D. This role ensures compliance with Novartis processes, ICH-GCP, and global regulatory requirements while delivering study outcomes within schedule, budget, and quality standards. The CSE I applies clinical data review principles to generate insights, identify trends, signals, and risks related to trial endpoints and patient safety. This role is a core member of the Clinical Trial Team (CTT) and may contribute to program-level activities as assigned.

Key Responsibilities:

  • Support the execution of global clinical trials, ensuring timely, efficient, and quality completion within budget and regulatory standards.

  • Perform clinical data review and provide actionable insights that meet Novartis quality standards and inspection readiness.

  • Assist with program-level activities, including tracking timelines, risk management, and operational planning.

  • Manage interactions with cross-functional teams such as Data Management, Drug Supply, Clinical Development, and Country Pharma Organizations.

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

  • Contribute to high-quality study documents, including protocols, informed consent forms, and clinical sections of regulatory submissions.

  • Ensure compliance with Novartis values: Innovation, Quality, Collaboration, Performance, Courage, and Integrity.

Key Performance Indicators (KPIs):

  • Consistent, accurate, and inspection-ready clinical data review.

  • High-quality contributions to clinical trial documentation.

  • Proactive operational planning with risk mitigation strategies.

  • Effective collaboration across cross-functional and global teams.

Minimum Requirements:

Experience:

  • Proven experience in clinical research and clinical trial execution.

  • Cross-cultural and multi-disciplinary team collaboration experience.

  • Project management and operational execution in clinical trial settings.

Skills & Competencies:

  • Expertise in clinical trial protocols, clinical data review, and risk monitoring.

  • Strong understanding of data integrity, trends analysis, and lifecycle management in life sciences.

  • Ability to collaborate effectively across organizational boundaries.

  • Learning design and scientific communication skills.

Languages:

  • Proficiency in English (written and spoken).

Why Join Novartis:
At Novartis, you will work in an environment that encourages innovation, collaboration, and personal growth. Join a community of passionate professionals dedicated to improving patient outcomes globally.

Benefits and Rewards:
Novartis provides a comprehensive suite of benefits and development opportunities to support your personal and professional growth. Learn more about Novartis benefits.

Equal Opportunity & Accessibility:
Novartis is committed to building inclusive teams that reflect the diversity of the patients and communities we serve. We provide reasonable accommodations to individuals with disabilities. If you require an accommodation during the recruitment process, please contact diversityandincl.india@novartis.com with the job requisition number.

Division: Research & Development
Business Unit: Development
Site: Hyderabad, India