Medical Fellowship at Novartis | Apply Now
Looking to advance your career through a medical fellowship? The Novartis Clinical Development Fellowship offers a unique 2-year opportunity for MD graduates to gain hands-on experience in global clinical trials. This program is ideal for candidates exploring Novartis careers, Novartis fellowships, and high-impact MD jobs in the pharmaceutical industry.
Job Details
- Job Position: Clinical Development Fellow
- Job ID: REQ-10074584
- Location: Hyderabad, India
- Program Start Date: September 1, 2026
- Duration: 2 years
- Application Deadline: April 6, 2026
About the Company
Novartis is a leading global healthcare organization focused on reimagining medicine to improve and extend people’s lives. With thousands of participants in clinical trials worldwide, Novartis is at the forefront of innovation in drug development, making it a top destination for Novartis careers and Novartis fellowships.
Job Description
Join the 2-year Clinical Development Postgraduate Fellowship at Novartis and gain hands-on experience contributing to global clinical studies from protocol to results. This medical fellowship provides exposure to multiple therapeutic areas including Oncology, Neuroscience & Gene Therapy, Global Health, Cardiovascular, Renal & Metabolism, and Immunology.
With nearly 50,000 participants in clinical trials, Novartis aims to ensure the right patients are enrolled in the right trials at the right time. This program is ideal for those seeking MD jobs and aiming to build a strong foundation in clinical development.
Qualifications
- Advanced degree (MD)
- Demonstrated interest in clinical development through coursework, internships, or training
- Strong curiosity and willingness to learn within the pharmaceutical industry
- Excellent interpersonal and communication skills
- Ability to work in multicultural and cross-functional teams
Key Responsibilities
- Acquire an understanding of Clinical Functions and Clinical Development Units
- Contribute to trial-related documents such as Clinical Trial Protocols (CTPs), informed consent forms, case report forms, and reports
- Support advisory boards, investigator meetings, and protocol training sessions
- Conduct ongoing medical and scientific review of clinical trial data
- Prepare and manage patient safety reports for safety and clinical boards
- Assist in final analyses, Clinical Study Reports, publications, and presentations
Important Information
- Applicants must be eligible to work in Hyderabad, India
- A cover letter is required, including:
- Motivation for the program
- Preferred development unit(s)
- Confirmation of availability from September 1, 2026
