Job Description Clinical Drug Development Postgraduate Training Program
46’000! That’s the number of patients in clinical trials at Novartis. Our vision in GDD is to engage these patients, making sure we have the right patients, in the right trials, at the right sites, at the right time. Do you want to use your expertise to help us reimagine medicine? Then we would like to hear from you for current and future opportunities within our development units for:
• Oncology / Hematology • Neuroscience • Global Health • Cardio-Renal-Metabolic • Ophthalmology • Immunology Hepatology & Dermatitis • Respiratory
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 addressing unmet needs and reimagining medicine? Do you have a collaborative mindset and take ownership of assigned tasks, and are you able to 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 an opportunity to discover the science of Clinical Development.
Your responsibilities: Your responsibilities include, but are not limited to: • 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 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 Medical Lead • Managing & preparing patient safety reports on trial data for use of 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
Duration and start of training: 2 years with an expected start date in September 2021
Minimum requirementsWhat you’ll bring to the role/ Minimum requirements:
• Advanced degree in life sciences is required, such as: Master Degree in one of the (bio) sciences, MPh, PhD, PharmD (completed within the last 2 years) • Clinical development training/class module at university/institution, knowledge of GCP, clinical trial design, statistics, and regulatory or clinical development exposure preferred • 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
Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks.
We are Novartis. Join us and help reimagine medicine.
Novartis is an equal opportunity employer committed to embracing and leveraging diverse backgrounds.
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