摘要
About the Role
Key Responsibilities
- Validate study designs and assess trial feasibility based on clinical practice and competitive analysis.
- Drive fast and high-quality trial site start-up through expert input during planning phases.
- Provide clinical expertise for IRB/EC interactions and informed consent content.
- Develop trial plans that address recruitment challenges and ensure data quality.
- Deliver robust training on indications, compounds, and protocols to internal and external stakeholders.
- Lead clinical recruitment strategies using physician insights and patient engagement.
- Support regulatory inspections and audits with scientific and clinical expertise.
- Ensure adherence to safety standards and provide medical input on adverse events.
Essential Requirements
- Advanced scientific degree (M.D. highly preferred; Ph.D. or Pharm.D. also considered).
- Strong understanding of clinical development processes and ICH/GCP guidelines.
- Minimum 3 years of experience in clinical development or clinical practice.
- Proven ability to lead cross-functional teams and resolve complex clinical issues.
- Excellent communication skills in English and the local language.
- Ability to deliver high-quality presentations and adapt across therapeutic areas.
Desirable Requirements
- Subspecialty training or experience with Real World Evidence (RWE).
- Familiarity with innovative study designs and data sources such as registries or electronic health records.
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? http://www.novartis.com/about/strategy/people-and-culture
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Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: http://www.novartis.com/careers/benefits-rewards
