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Novartis Life Sciences Clinical Scientific Expert Recruitment – Apply Now
About the Company:
Novartis is a global healthcare company dedicated to reimagining medicine for patients worldwide. With a focus on innovation and scientific advancements, Novartis strives to improve and extend people’s lives through the development of groundbreaking solutions. The company believes in the power of collaboration, diversity, and an unbossed culture to drive progress in the medical field. By joining Novartis, you have the opportunity to make a meaningful impact and tackle the world’s toughest medical challenges.
Position: Clinical Scientific Expert – I
Location: Hyderabad, AP, India
Job Type: Full Time
Employment Type: Regular
About the role:
As a Clinical Scientific Expert, you will be part of the Global Drug Development (GDD) team, responsible for maintaining the highest quality clinical trial data and regulatory reports throughout the life cycle of each program. Your role will involve providing clinical and scientific inputs at both the study and program level, collaborating with cross-functional teams to ensure the integrity and safety of clinical data. Additionally, you will contribute to the development of study-level documents and support pharmacovigilance activities when required.
Responsibilities include, but are not limited to:
- Ensuring high-quality clinical trial data review/insights and analysis as directed by the Integrated Clinical Trial Team (iCTT)
- Performing clinical data review at a patient level, identifying insights and trends, and facilitating resolution of clinical data issues
- Contributing to the development of the Data Review/Quality Plan (DRP/DQP) and data review strategy
- Collaborating with relevant line functions to enhance the quality of clinical data review/insights
- Supporting the development of study-level documents, including clinical sections of key regulatory documents
- Contribute to process improvements and the implementation of innovative data analysis processes and tools
- Providing training and support to the iCTT team
Role Requirements:
- Advanced degree in life sciences/healthcare or a clinically relevant field (Master’s, PharmD, M.Pharma, PhD, MBBS, BDS, MD strongly preferable)
- Fluent in English (oral and written)
- More than 1 year of experience in the pharmaceutical industry/clinical research organization
- Basic knowledge of planning, executing, reporting, and publishing global clinical studies
- Experience in clinical operations is preferred
- Strong interpersonal skills and ability to work under pressure
- Good negotiation and conflict resolution skills
- Fundamental knowledge of Good Clinical Practice, clinical trial design, statistics, and regulatory processes
- Demonstrates strong medical/scientific writing skills
- Knowledge and application of statistical analysis methodology
Why Novartis?
At Novartis, we believe in making a difference in the lives of patients and pushing the boundaries of medical science. By joining our team, you will be part of a dynamic and diverse environment that fosters innovation and growth. We encourage collaboration, integrity, and a constant pursuit of excellence. Together, we can reimagine medicine and create a positive impact on a global scale.
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