Clinical Data Specialist I

Novartis; Hyderabad; On-site; INR 900,000 - 1,500,000; Full time

Job summary

Novartis in Hyderabad, India seeks a Clinical Data Specialist I to provide clinical and scientific support across all study phases under guidance, ensuring data quality and compliance. You will apply data review principles to identify trends and risks and contribute to study deliverables.

The CDS I collaborates with data management, drug supply management, clinical development, and local country teams to ensure timely, compliant study execution and robust data integrity.

Qualifications

• Responsible for clinical data review to ensure data plausibility and to identify trends, signals and risks.
• Support program level activities and ensure data is compliant with ICH GCP.
• Collaborate with data management, drug supply management, and clinical development teams.

Responsibilities

• Implement issue resolution plans.
• Assist with program level activities (e.g., tracking).
• Manage interactions with relevant line functions including data management, drug supply management, and clinical development; report technical complaints/adverse events within 24 hours.
• Ensure timely, efficient, and quality execution of trial-related activities within budget and quality standards.

Skills

Clinical data review

Data integrity

Cross-functional collaboration

Project management

Job description

Contributes, with appropriate oversight, to all relevant aspects of global clinical trial(s) activities to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial(s). Core member of the Clinical Trial Team.

Applicable to Clinical Data Specialist I, The Clinical Data Specialist I (CDS I) provides clinical and scientific support through all phases of a clinical study under the guidance of the (A)CD(M)D in compliance with Novartis processes, ICH GCP and regulatory requirements. This role applies the principles of clinical data review excellence and identifies clinical data insights to ensure data is scientifically plausible and to identify trends, signals and risks associated to trial endpoints and patient safety. The CDS I is a core member of the Clinical Trial Team (CTT) and may support program level activities as assigned.

Implementing issue resolution plans; -Assist with program level activities (e.g., tracking of program -Managing interactions with relevant line functions including data management, drug supply management, clinical development and/or Novartis Country Pharma Organizations; -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)

Timely, efficient and quality execution of assigned trials and trial related activities within budget, and in compliance with quality standards.Proactive operational planning with effective contingency and risk mitigation plans.

-Performing clinical data review and insights consistently and accurately which meets the Novartis quality standards, timelines, and is inspection ready.High quality contributions to study documents (e.g. protocol, ICF, clinical sections of CTA) -Clearly demonstrates Novartis Values and Behaviors (i.e. Innovation, Quality, Collaboration, Performance, Courage and Integrity)

Work Experience: Cross Cultural Experience.Operations Management and Execution.Collaborating across boundaries.Project Management.SkillsClinical Research.Clinical Trial Protocol.Clinical Trials.Data Integrity.Learning Design.Lifesciences.Risk Monitoring.Trends Analysis.LanguagesEnglish.

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