vor 4 Tagen

Lead Biostatistics

Philip Morris International

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Are you up for a challenge? Do you look for ways to grow in your job? And do you want to build a phenomenal career? Then apply now! We’re currently looking for a:

Lead Biostatistics

Are you up for a challenge Do you look for ways to grow in your job And do you want to build a phenomenal career Then apply now We're currently looking for a Lead Biostatistics We don't just want any Lead here is our checklist



M Sc or PhD in statistics related field.


Knowledge and experience designing and implementing clinical trials observational research and conducting statistical analysis e.g. experimental design power sample size handling of missing data hypothesis testing.


Substantial experience setting up and overseeing data analysis of clinical trials within a regulated environment ICH GCP CDISC .


Experience regulatory and scientific interactions and engagement.


Experience in in managing projects managing teams and CROs.


Fluent in English.



If you are detail oriented good with deadlines a team player and comfortable with different levels of stakeholders and management while operating in a changing environment you are the one we want for our Health Outcomes Biostatistics Department in Philip Morris Products S.A. Research Development R D in Neuchâtel Switzerland.

The objective of Philip Morris International Inc. PMI 's R D team is to develop and assess products with the potential to reduce the risks of smoking-related diseases. This project is at the core of our business and our aim is that one day all adult smokers who otherwise wouldn't quit will switch to what we call reduced-risk products RRPs . Get to know more about us on www.PMIScience.com.

As the Lead Biostatistics you will bridge the scientific and regulatory needs with the business needs ndash integrating the statistical methodology with the clinical science regulatory requirements and market/competitive intelligence. When functioning in a supervisory role you will provide guidance and mentor staff while overseeing the technical evolution of the department. You may also represent the department for internal and external engagement during scientific and regulatory meetings and audits.

Specific responsibilities include


In collaboration with clinical scientific and medical counterparts ensure that the statistical approach and analysis strategies are robust and aligned with the regulatory and business objectives.


Contribute to the clinical development and study execution strategy including the product assessment plan to define the clinical assessment safety surveillance and post-market assessment programs.


Work across multiple studies across product platforms with the responsibility for fully integrating the statistical strategy and interpretation over the entire product lifecycle.


Manage and oversee the CROs selected to operationalize the studies with focus on the governance to ensure the quality and timeliness of the deliverables across the entire program


Interact with senior management scientific advisors and external key opinion leaders for quantitative aspects of the program and identify opportunity for contributing to publications and white papers.


Manage a team of statisticians data analysts and statistical programmers internally.



Why work for us Here are 3 reasons PMI is the ultimate Employer to unlimit yourself

1. We're international you work with clients and learn on-the-job from team members from all over the world
2. We're flexible your work fits you and not the other way round thanks to our Flexible Work Arrangement Program and
3. We're a certified top employer we consider our employees to be our strongest asset and we are developing talent throughout all levels of the organization.

And rest assured as the first multinational company in Switzerland to obtain the Equal-Salary label for men and women our competitive salary and compensation package is for all our employees

JOIN A GLOBAL MARKET LEADER

If you wish to contribute to the future of our business and to the new scientific journey of the industry please apply online.

PMI is the world's leading international tobacco company with six of the world's top 15 international brands and products sold in more than 180 markets. In addition to the manufacture and sale of cigarettes including the number one global cigarette brand and other tobacco products PMI is engaged in the development and commercialization of Reduced-Risk Products ldquo RRPs rdquo . RRPs is the term we use to refer to products that present are likely to present or have the potential to present less risk of harm to smokers who switch to these products versus continued smoking. We have a range of RRPs in various stages of development scientific assessment and commercialization. Because our RRPs do not burn tobacco they produce far lower quantities of harmful and potentially harmful compounds than found in cigarette smoke. For more information see www.pmi.com and www.pmiscience.com.

PMI is an Equal Opportunity Employer.

A valid Swiss work permit or Swiss or EU-25/EFTA citizenship is required for this position.

PMI affiliates do not accept referrals from employment agencies in respect of the vacancies posted on this site. Should an employment agency take any action in respect of such a vacancy their actions will have been taken without the request or agreement of any PMI affiliate no PMI affiliate shall be liable for any fees in such circumstances.