Associate Director Biostatistics

Our Development Team is guided by our purpose: to reimagine medicine to improve and extend people’s lives.

To do this, we are optimizing and strengthening our processes and ways of working. We are investing in new technologies and building specific therapeutic areas and platform depth and capabilities – all to bring our medicines to patients even faster.

We are seeking key talent, like you, to join us and help give people with disease and their families a brighter future to look forward to.

Apply today and welcome to where we thrive together!

The Role:

We are seeking a highly skilled and motivated individual to join our team as Associate Director of Biostatistics. You will be required to influence and drive the statistical strategy/innovation directly taking part in cross-functional collaboration and decision making for program(s) across (pre/early/full) clinical development and/or medical affairs. You will have proven experience in supporting complex clinical trials and leading strategy through collaborations with partners across the drug development organization.

This role may be in Early Development, Preclinical or Global Medical Affairs

Key responsibilities:

• Responsible for all statistical tasks on assigned clinical trials, with a high level of independence seeking peer input/review as required. Responsible for protocol development in alignment with the clinical development plan, developing statistical analysis plan, and leading study- and indication-level reporting activities.

• Contribute to planning and execution of exploratory analyses, innovative analyses related to publications and pricing & reimbursement/submission and/or PK, PK/PD analyses, exploratory biomarker and diagnostic analyses, and statistical consultation. Initiate, drive, and implement novel methods and innovative trial designs and dose-finding strategies in alignment with the Lead Statistician.

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  Independently lead interactions with external review boards/ethics committees, external consultants, and other external parties with oversight as appropriate. Represent Novartis in statistical discussions at external congresses, conferences, scientific meetings.

• Represent the Biostatistics & Pharmacometrics Line Function on cross-functional teams for the assigned trials. Responsible for functional alignment and ensuring line function awareness throughout the trials.

• Collaborate with other line functions. Explain statistical concepts in an easily understandable way to non-statisticians and provide adequate statistical justifications and interpretation of analysis results for actions/decisions/statements, when required.

• Establish and maintain collaborative relationships and effective communications within the Clinical Trial Team and Biostatistics & Pharmacometrics team.

• Independent oversight of Biostatistics resources and deliverables for assigned trials.

• Ensure all Biostatistics deliverables for assigned clinical trials and/or non-clinical related activities are delivered in a timely manner with the highest level of quality.

Your Experience:

• MS Statistics with 10 years’ work experience or PhD (in Statistics or equivalent) with 6years work experience

• Fluent in English with strong communication and presentation skills, with the ability to articulate complex concepts to diverse audiences.

• Effective utilization of innovative statistics and quantitative analytics to influence assigned program team decisions and support department to deliver objectives.

• Proven knowledge and expertise in statistics and its application to clinical trials. Depending on the assignment, may require proven expertise in pharmacokinetics, exposure-response modelling, exploratory biomarker, diagnostic analyses, applied Bayesian statistics, or data exploration skills. Demonstrated excellence in use of statistical software packages (e.g. SAS, R). Strong knowledge of drug development and Health Authority guidelines. Experience independently leading a multidisciplinary team to achieve team objectives. Expert skills to facilitate and maximize the contribution of quantitative team. Hands-on experience in leading the interface to regulatory agencies/leading the early clinical development campaign.

• Experience in providing statistical expertise to support submission activities, including documents, meetings with and responses to Health Authorities, pricing agencies and drug development activities, as required.

• Strong understanding of Franchise/Therapeutic Area and/or regulatory activities in at least one disease area.

• Expert scientific leadership skills demonstrated in facilitating and optimizing the clinical development strategy.

• Strong track record for global scientific leadership in the development and evaluation of modern program/trial design methodologies.

• Demonstrated strong skills in building partnerships and collaborations. Ability to mentor for up to 8 associates.

• This role offers hybrid working, requiring 3 days per week or 12 days per month in our London Office.

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

Commitment to Diversity & Inclusion:

Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.

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