Job Description
This job is with Novartis, an inclusive employer and a member of myGwork – the largest global platform for the + business community. Please do not contact the recruiter directly.
Summary
The Protocol & Clinical Program Excellence Director will provide strategic, scientific planning and operational support to the Head of Protocol & Clinical Program Excellence to achieve the CD program goals aligned with the overall CD strategy and vision.
The role will support scientific and operational activities of the CD Central Integrated Scientific Review Committee (C-ISRC) and collaborate closely with the Head Protocol & Clinical Program Excellence, C-ISRC Leads, CD(M)Ds, trial teams, and cross-functional partners as needed.
This position is based in the UK / London with a hybrid working model.
About the Role
1. Provide scientific and operational support to the C-ISRC, including reviewing Clinical Development Plans (CDPs) and key clinical documents (e.g., study protocols, DMC charters) to ensure high quality and consistency across therapeutic areas.
2. Develop harmonized processes, tools, and resources to facilitate seamless C-ISRC operations.
3. Support activities like interactions with external stakeholders (regulatory authorities, key opinion leaders, data monitoring committees, advisory boards) and internal stakeholders, acting as a delegate to the Head Protocol & Clinical Program Excellence.
4. Assist in enhancing and simplifying Novartis's clinical development approach to improve trial speed and success outcomes.
5. Engage with CD(M)Ds and the broader CD community to share clinical learnings and support professional development strategies.
6. Support strategic initiatives for cross-functional collaboration and the transition to digital clinical trials.
Education and Minimum Experience
* MD or advanced degree in life sciences/healthcare (or clinically relevant degree), such as PharmD or PhD.
* Over 5 years of experience in clinical research or drug development across phases I-IV in academic or industry settings.
* More than 3 years of experience conducting clinical trials, including planning, execution, reporting, and publishing in a global/matrix environment.
* Excellent interpersonal, negotiation, conflict resolution, and communication skills.
* Strong influencing skills without formal authority.
* Fluent in oral and written English.
Why Novartis
Helping people with disease and their families requires more than innovative science. It takes a community of passionate, collaborative individuals like you. Join us to make a difference and create a brighter future together.
Learn more about our people and culture
Commitment to Diversity
Novartis is dedicated to building an inclusive, diverse workplace that reflects the communities we serve.
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Benefits and Rewards
Discover how we support your personal and professional growth: https://www.novartis.com/careers/benefits
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