Clinical Scientific Expert I

Job title:

Clinical Scientific Expert I

Company

Novartis

Job description

Job Description Summary Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly.The Clinical Scientific Expert 1 (CSE) 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 CSE I is a core member of the Clinical Trial Team (CTT) and will support program level activities as assigned.Job DescriptionKey responsibilities:Perform high quality clinical data review, and identify clinical data insights through patient level review and trend analysis, supporting interim analysis, Database Lock activities, Emphasis on subject safety and eligibility, data integrity, trend identification, analysis, and remediationContribute to development of Data quality review plan (DRP), and data review strategyMay contribute to Protocol development, and CRF development.Contribute to and facilitate data review process enhancements, and implementation of innovative data analysis processes and tools.May contribute to study level documents and submission dossiersMay support pharmacovigilance activitiesLocation: #LI-Hybrid Dublin officeEssential requirements:Msc in life sciences, ideally PHD/MD qualification.Scientific, strategic and operational experience in planning, executing, reporting and publishing clinical studies in industry or academia.Skills Desired Budget Management, Clinical Research, Clinical Trial Protocols, Clinical Trials, Coaching, Data Analysis, Data Integrity, Learning Design, Life Science, Risk Monitoring, Trend Analysis

Expected salary

Location

Dublin

Job date

Thu, 19 Jun 2025 07:04:06 GMT

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