Clinical Development Postgraduate Fellow
Vor 3 Tagen
Job ID REQ-10042760
Mar 04, 2025
SummaryThe Clinical Development Postgraduate Training Program is a unique opportunity to discover the science of Clinical Development during a two-year program starting September 1, 2025.
About the RoleWith nearly 50,000 patients in clinical trials at Novartis, our vision in Clinical Development is to engage these patients, making sure we have the right patients, in the right trials, at the right sites, at the right time.
After your Master's, Doctoral or Post-doctoral qualification, do you want to learn more about and gain more experience in Clinical Development at a leading global healthcare company and see how drugs are developed to help address unmet needs and reimagine medicine? Do you have a collaborative mindset, take ownership of assigned tasks, and can quickly adapt to different multicultural teams and diverse concepts? Besides that, do you have excellent problem-solving skills?
The Clinical Development Postgraduate Training Program is a unique opportunity to discover the science of Clinical Development in one of our development units:
- Neuroscience & Gene Therapy
- Cardiovascular, Renal & Metabolism
Start: September 1, 2025
Duration: 2 years
Important: Please submit a cover letter that includes your motivation for the program, explains which development unit(s) you are most interested in, and confirms your availability for a start on September 1, 2025. Thank you.
Your responsibilities include:
- Acquiring an understanding of the organization, how Clinical Functions and Clinical Development Units work together to develop solutions that address unmet needs for patients and discover the science of clinical development.
- Contributing to the development of trial-related documents (e.g., Clinical Trial Protocols (CTPs), informed consent form, case report forms, data analysis plan, data monitoring committee charters, reports, publications) for assigned clinical trial(s) consistent with the Clinical Development Plan. May include developing materials for trial-related advisory boards, data monitoring committees, investigators meetings, and protocol training meetings for Novartis local & global medical organizations.
- Conducting ongoing medical, clinical, and scientific review of clinical trial data with Clinical Scientific Expert(s) with appropriate oversight from the Medical Lead.
- Managing & preparing patient safety reports on trial data for use by safety and clinical boards (e.g., Safety Management Team, Global Clinical Team, Global Program Team) with appropriate oversight from the Medical Lead.
- Providing input into final analyses and interpretation including the development of the Clinical Study Report(s), publications, and internal/external presentations.
What you'll bring to the role:
- Advanced degree in life-sciences is required, such as: Master Degree in one of the (bio) sciences, MPh, PhD, PharmD or MD (completed within the last 2 years).
- Concrete interest in clinical development as demonstrated by training/class module at university/institution, internships or specific courses.
- Seeking new and different experiences for learning in the pharmaceutical industry and curiosity about clinical development.
- Strong interpersonal skills i.e. can demonstrate your ability to communicate well and establish effective working relationships with people from a variety of backgrounds/cultures and at different hierarchical levels inside and outside the company.
Accessibility and accommodation:
Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion_ch@novartis.com, and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
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