Clinical Research Job at Novartis
Professionals searching for Clinical Research Job can explore the Clinical Scientific Expert-I opportunity at Novartis in India. This full-time role within Research & Development involves clinical data review, global clinical study support, regulatory documentation, and patient-safety activities. Candidates with an advanced healthcare or life sciences degree and 1–2 years of relevant clinical study experience can explore this opportunity under Novartis Careers.
About Novartis:
Novartis is a global medicines company headquartered in Switzerland with research and development activities spanning multiple therapeutic areas. The company develops innovative medicines and conducts clinical research to evaluate their safety and effectiveness. This position sits within the Development division and provides an opportunity to contribute to clinical studies and drug-development activities within a global pharmaceutical environment.
Job Details:
- Position: Clinical Scientific Expert-I
- Company: Novartis
- Job ID: REQ-10087559
- Location: Hyderabad, India
- Functional Area: Research & Development
- Job Type: Full-Time
- Employment Type: Regular
- Shift Work: No
Job Description:
Novartis is looking for a Clinical Scientific Expert-I to provide clinical and scientific support across different phases of clinical studies under appropriate medical and clinical development guidance. The position involves reviewing patient-level clinical data, identifying trends, signals and potential risks, supporting clinical trial documentation, and contributing to data-review strategies. The Clinical Scientific Expert-I will work as a core member of the Clinical Trial Team while ensuring compliance with Novartis processes, ICH-GCP, and applicable regulatory requirements.
Key Responsibilities:
Candidates selected for these Clinical Research Job will be responsible for:
- Performing high-quality clinical data reviews.
- Reviewing patient-level clinical information and identifying meaningful clinical insights.
- Analysing clinical data for trends, signals, and potential risks.
- Assessing whether clinical data is scientifically plausible.
- Supporting the identification of issues related to trial endpoints and patient safety.
- Supporting Interim Analysis, Database Lock, and Post-Lock activities.
- Facilitating the resolution of clinical data issues.
- Contributing to Data Review/Quality Plans (DRP/DQP).
- Supporting the development of clinical data-review strategies.
- Contributing to Case Report Form development.
- Supporting implementation of clinical data-capture tools.
- Identifying opportunities to improve data-review processes.
- Contributing to study-level documents and clinical sections of key regulatory documents.
- Supporting pharmacovigilance activities when required.
- Developing training materials and providing training to relevant Clinical Trial Team members.
- Developing subject-matter expertise in therapeutic areas and clinical data-review tools.
Educational Requirements:
Candidates should possess an advanced degree in Life Sciences, Healthcare, or another clinically relevant discipline.
Qualifications strongly preferred by Novartis include:
- MBBS
- BDS
- MD
Applicants should ensure their academic background satisfies the exact requirements of the official Novartis listing.
Experience Required for this Clinical Research Job:
Candidates should have approximately 1–2 Years of Relevant Experience
The role requires scientific, strategic, and operational experience involving:
- Planning clinical studies
- Executing clinical studies
- Reporting clinical studies
- Publishing clinical studies
Applicants should also possess an intermediate understanding of global clinical study planning, execution, reporting, and publication.
This should not be marketed as a fresher position, since relevant professional experience is specifically requested.
Skills Required for this Clinical Research Job:
Candidates interested in a Clinical Research Job at Novartis should possess:
- Clinical Data Review
- Clinical Trial Knowledge
- ICH-GCP Knowledge
- Drug Development Knowledge
- Clinical Data Analysis
- Scientific Interpretation
- Problem-Solving Skills
- Communication & Presentation Skills
- Attention to Detail
- Cross-Functional Collaboration
