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- 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 ÂŁ per year.
Join to apply for the Precision Medicine Associate Director role at Novartis
Join to apply for the Precision Medicine Associate Director role at Novartis
Summary
The Precision Medicine Associate Director (PMaD) provides clinical drug development, scientific and technical expertise for successful implementation and execution of the Precision Medicine plans for clinical studies in a given program with a focus on ensuring timely execution to meet studies timelines.
Summary
The Precision Medicine Associate Director (PMaD) provides clinical drug development, scientific and technical expertise for successful implementation and execution of the Precision Medicine plans for clinical studies in a given program with a focus on ensuring timely execution to meet studies timelines.
Primary Location: London, UK
Other Locations: Dublin, Ireland
Relocation Support: This role is based in London/Dublin. Novartis is unable to offer relocation support: please only apply if accessible.
Responsibilities
About the Role
- Serves as core member of the BDST and as subject matter expert at the Global Clinical Team (GCT) and/or Clinical trial team (CTT) as applicable. 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 the study protocols and clinical study reports.
- Avoids strategic and operational crises by proactively identifying and managing potential risks to the program(s) and communicate them timely to GCT/CTT to minimize impact on program.
- Supports regulatory submissions by acting as biomarker/clinical Dx subject matter expert within the GCT/CTT team.
- Partners with CBS and other internal stakeholders to ensure all aspects of data collection and analysis are executed with high quality including statistical analysis plan, data formatting and transfer specifications, eCRF page design, and monitoring plans for biomarker study samples.
- May Support exploratory/scientific external academic collaborations to support biomarker data generation.
- Ensures Compliance to applicable US and international Medical Device regulations and standards including, but not limited to, 21 CFR 820, ISO 13485, 93/42/EEC, 98/79 EC, and the requirements of the Novartis CDx Quality Management System.
Essential For The Role
- Education: MD or Ph.D. OR MD/Ph.D. with minimum of 6 years of experience in the field of precision medicine including CDx/IVD and minimum of 3 years in the pharmaceutical industry.
- 3+ years multi/cross functional leadership experience within either or Oncology, Immunology, Neuroscience, Cardiometabolic business unit.
- Excellent knowledge of diagnostics and associated regulatory requirements
- Expert leadership skills demonstrated in cross functional teams.
- Expert skills to facilitate/optimise contribution of team members as individuals and member of cohesive team.
Commitment To Diversity & Inclusion
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
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? our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally:
Seniority level
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Seniority level
Mid-Senior level
Employment type
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Employment type
Full-time
Job function
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Job function
Business Development and Sales
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Industries
Pharmaceutical Manufacturing
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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.
