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For Companies At a Glance
- Tasks: Lead clinical drug development and ensure timely execution of Precision Medicine plans.
- Company: Join Novartis, a global leader in innovative pharmaceuticals dedicated to improving patient lives.
- Benefits: Enjoy personal and professional growth opportunities in an inclusive work environment.
- Why this job: Be part of a passionate team making breakthroughs that change patients' lives.
- Qualifications: MD or Ph.D. with 6+ years in precision medicine and leadership experience required.
- Other info: Work from London or Dublin in a full-time role with no shift work.
The predicted salary is between 43200 - 72000 £ per year.
Summary
The Precision Medicine Associate Director (PMaD) provides clinical drug development, scientific, and technical expertise for the successful implementation and execution of the Precision Medicine plans for clinical studies within a program. The role focuses on ensuring timely execution to meet study timelines.
About the Role
Responsibilities:
- Serves as a core member of the BDST and as a subject matter expert at the Global Clinical Team (GCT) and/or Clinical Trial Team (CTT), as well as externally (e.g., steering committees).
- Contributes to the Dx target product profile (DxTPP) and the overall IVD/CDx development strategy and plan.
- Authors the biomarker/CDx portions of study protocols and clinical study reports.
- Proactively identifies and manages potential risks to avoid strategic and operational crises, communicating them timely to GCT/CTT to minimize impact.
- Supports regulatory submissions by acting as a biomarker/clinical Dx subject matter expert within the GCT/CTT team.
- Partners with CBS and other internal stakeholders to ensure high-quality data collection and analysis, including statistical analysis plans, data formatting, transfer specifications, eCRF design, and monitoring plans for biomarker study samples.
- Supports exploratory/scientific external academic collaborations to support biomarker data generation.
- Ensures compliance with applicable US and international Medical Device regulations and standards, including 21 CFR 820, ISO 13485, 93/42/EEC, 98/79 EC, and the Novartis CDx Quality Management System.
Essential for the role:
- MD or Ph.D., or MD/Ph.D. with at least 6 years of experience in precision medicine, including CDx/IVD, and a minimum of 3 years in the pharmaceutical industry.
- Over 3 years of multi/cross-functional leadership experience within Oncology, Immunology, Neuroscience, or Cardiometabolic units.
- Excellent knowledge of diagnostics and regulatory requirements.
- Demonstrated leadership skills in cross-functional teams.
- Ability to facilitate and optimize contributions of team members both individually and as part of a cohesive team.
Commitment to Diversity & Inclusion:
Novartis is dedicated to building an outstanding, inclusive work environment with diverse teams that reflect the patients and communities we serve.
Why Novartis: Helping people with disease and their families requires more than innovative science. It takes a community of passionate, smart people like you. Collaborate, support, and inspire each other to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? Learn more
Join our Novartis Network: Not the right role for you? Sign up to our talent community to stay connected and learn about new opportunities:
Benefits and Rewards: Read our handbook to discover how we support your personal and professional growth:
Division: Development Business Unit: Universal Location: London, UK; Dublin, Ireland Company: Novartis Pharmaceuticals UK Ltd Employment Type: Full-time, Regular Shift Work: No
Novartis is committed to building an outstanding, inclusive work environment and diverse teams that reflect the patients and communities we serve.
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Precision Medicine Associate Director employer: Novartis
Contact Detail:
Novartis Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Precision Medicine Associate Director
✨Tip Number 1
Network with professionals in the precision medicine field, especially those who have experience in clinical drug development. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends and challenges in the sector.
✨Tip Number 2
Familiarise yourself with the specific regulatory requirements mentioned in the job description, such as 21 CFR 820 and ISO 13485. Understanding these regulations will not only enhance your knowledge but also demonstrate your commitment to compliance during interviews.
✨Tip Number 3
Prepare to discuss your leadership experiences in cross-functional teams, particularly in Oncology, Immunology, Neuroscience, or Cardiometabolic units. Be ready to provide examples of how you've facilitated team contributions and managed risks in previous roles.
✨Tip Number 4
Showcase your passion for diversity and inclusion in your conversations with the hiring team. Research Novartis' initiatives in this area and be prepared to discuss how you can contribute to building an inclusive work environment.
We think you need these skills to ace Precision Medicine Associate Director
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in precision medicine, clinical drug development, and leadership roles. Use specific examples that demonstrate your expertise in diagnostics and regulatory requirements.
Craft a Compelling Cover Letter: Write a cover letter that clearly outlines your passion for precision medicine and how your background aligns with the responsibilities of the Precision Medicine Associate Director role. Mention your experience with cross-functional teams and any significant contributions you've made in previous positions.
Highlight Relevant Skills: In your application, emphasise skills such as risk management, data analysis, and compliance with medical device regulations. Provide concrete examples of how you've successfully applied these skills in past roles.
Showcase Leadership Experience: Detail your leadership experience within multi/cross-functional teams, particularly in Oncology, Immunology, Neuroscience, or Cardiometabolic units. Highlight specific projects where you facilitated team contributions and achieved successful outcomes.
How to prepare for a job interview at Novartis
✨Showcase Your Expertise
As a Precision Medicine Associate Director, it's crucial to demonstrate your deep understanding of clinical drug development and precision medicine. Be prepared to discuss your previous experiences in detail, especially those related to CDx/IVD and how you've contributed to successful clinical studies.
✨Highlight Leadership Experience
This role requires strong leadership skills within cross-functional teams. Share specific examples of how you've led teams in the past, particularly in Oncology, Immunology, Neuroscience, or Cardiometabolic units, and how you facilitated collaboration among team members.
✨Understand Regulatory Requirements
Familiarise yourself with relevant regulations such as 21 CFR 820 and ISO 13485. During the interview, be ready to discuss how you've ensured compliance in previous roles and how you can apply this knowledge to support regulatory submissions effectively.
✨Emphasise Problem-Solving Skills
The ability to identify and manage potential risks is key in this position. Prepare to share instances where you've proactively addressed challenges in clinical studies, detailing the strategies you employed to mitigate risks and ensure timely execution.
