Company: Novartis
Location: India
Salary: INR 25,000 – 35,000 per month
Qualifications: PharmD, M.Pharma, PhD, MBBS, BDS, MD, MSc
Experience: 1 to 2 Years
Job Description:
Join Novartis’ Global Drug Development team as a Clinical Scientific Expert I. Contribute to ensuring top-quality clinical trial data across all disease areas, supporting our mission to advance medicine globally.
Key Responsibilities:
| Responsibilities | Details |
|---|---|
| Ensure high-quality clinical trial data review, insights, and analysis. | Analyze patient-level data, identify trends, and support Interim Analysis and Database activities. |
| Collaborate with Integrated Clinical Trial Team (iCTT) to resolve data issues. | Enhance data review quality focusing on subject safety, eligibility, and integrity. |
| Contribute to Data Review/Quality Plans (DRP/DQP) and data review strategies. | Ensure protocol adherence and contribute to CRF development and data capture tools. |
| Support development of study-level documents and regulatory submissions. | Assist in creating clinical sections for regulatory documents and publications. |
| Drive process improvements in data review and analysis. | Innovate data analysis processes and tools. |
| Assist in pharmacovigilance activities and safety monitoring. | Review aggregate reports and attend Safety Monitoring Meetings (SMT) as required. |
| Develop training materials and provide training to iCTT. | Facilitate knowledge transfer and skill development within the team. |