Associate Job at Novartis – Jobs for Medical Graduates | Apply Now
Looking for impactful jobs for medical graduates that combine research, innovation, and real-world medical application? Explore the Associate Job at Novartis in Translational Clinical Oncology (TCO). This position allows you to contribute to early-phase cancer studies that shape the future of oncology treatments. Join a world-class biomedical research team where science meets purpose, and every discovery can change a patient’s life.
- Job ID: REQ-10047661
- Job Position: Associate Medical Expert
- Department: Translational Clinical Oncology (TCO)
About the Company:
Novartis is a global leader in healthcare innovation, dedicated to improving and extending people’s lives. The Translational Clinical Oncology (TCO) division under its Biomedical Research arm focuses on early-phase cancer studies, bridging drug discovery and late-phase development. By joining the Associate Job at Novartis, you become part of a passionate global community driven by science, collaboration, and the mission to deliver life-changing therapies – making it one of the most fulfilling jobs for medical graduates in oncology research.
Qualifications:
- Education: MD or equivalent medical degree with medical council certification.
- Experience: Minimum 2 years in the pharmaceutical/biotech industry or 4 years in hospital clinical practice.
- Preferred: Background in hematology or oncology.
- Knowledge: Clinical operations, regulatory documentation, and Good Clinical Practice (GCP).
Job Description:
The Associate Job at Novartis in the Translational Clinical Oncology (TCO) team offers a unique opportunity to contribute to global and long-term oncology studies. The role supports the Clinical Program Leader (CPL) and Medical Expert in designing, executing, and evaluating innovative cancer therapies that bridge the gap between laboratory research and clinical application.
Key Responsibilities:
- Provide medical and scientific support to Clinical Program Leaders and Medical Experts.
- Contribute to clinical sections of protocols, informed consents, and regulatory documents.
- Support medical monitoring and safety reporting for ongoing oncology studies.
- Review clinical trial data to ensure quality and scientific integrity.
- Lead or assist in clinical study reports (CSR), publications, and health authority submissions.
- Participate in dose escalation meetings, investigator calls, and site initiation visits.
- Maintain compliance with ICH-GCP, Novartis SOPs, and global regulatory standards.
- Uphold Novartis values by promoting collaboration, innovation, and continuous improvement.
