摘要
About the Role
HSEMajor accountabilities:
- CTSM will be responsible for study supply leadership to ensure timely planning and execution of supply strategy for continued supply of clinical finished goods (supply drugs) to patients.
- Study managers provides inputs in clinical study protocol, understand study design and are responsible for optimal clinical trial supply strategy in terms of packaging design, pro- active planning following a risk-based approach
- Represent Global Clinical Supply as a single point of contact (SPOC) at trial level for the integrated Clinical Trial team (iCTT).
·Accountability and leadership
- Self awareness
- Open to seek and receive feedback
- Having Right attitude
·Operational & Project excellence
- Proactive in study planning and assigned portfolio
- Ensures to have robust risk management (identification and mitigation of risks) and various scenario to support decision making process
- Able to navigate through current processes and procedures , while focusing on continuous improvement
- Setting priorities and holding self and others accountable to meet commitments.
·Stakeholder management & Interpersonal skills
- Able to engage, influence, align and lead internal and external business partners
- Ability to work well with diverse groups of people, handles conflict & challenging situations effectively and builds formal and informal relationships
·Communication Skills & Business mindset
- Able to communicate effectively with different audiences
- Ability to consider business necessities and financial indicators when taking decisions and or/managing budgets.
·Managing Change
- Ability to effective rebound from set-backs and adversity when facing difficult situations
- Ability to adopt to different situations and to operate effectively during times of uncertainty.
Minimum Requirements:
Work Experience:
- Functional Breadth.
- Managing Crises.
- People Challenges.
- Collaborating across boundaries.
- Operations Management and Execution.
- Project Management.
- 3-4 years relevant experience.
Skills:
- Advanced Project Management.
- Supply Chain Planning.
- Supply-Chain Management.
- Data & Digital Savviness with high learning agility
- Knowledge of relevant regulations (GMP, HSE)
Languages :
- English.
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? https://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: https://www.novartis.com/careers/benefits-rewards
Accessibility and accommodation
Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
