Principal Biostatistician, HTA Statistics
Regus, Zurich, Switzerland
vor 5 Tg.

Job Description

We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we follow the science and that great medicines can make a significant impact to our world.

And we believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.

You will be part of the BARDS organization which has a presence in the US, Europewide and Asia Pacific. By joining our company, in this role you will apply your skills and experience in support of developing scientifically based arguments aiming to provide fair accessibility to our company’s drugs and vaccines making a real difference in patient’s lives.

The Biostatistics and Research Decision Sciences (BARDS) organization has a proud record of providing comprehensive analytical and methodological expertise to support our company’s strategic goals.

Our quantitative scientists aspire to maintain the highest quality output while adopting the most efficient and effective scientific and operational procedures that will promote breakthrough innovation, collaboration and professional activity.


We are currently seeking a Principal Biostatistician, HTA Statistics to be part of the BARDS organization in Zurich. In this role you will apply your skills and experience in support of developing scientifically based arguments aiming to provide fair accessibility to the company s drugs and vaccines making a real difference in patient’s lives.

Key responsibilities for the position

  • Provides statistical leadership and support to projects in the BARDS HTA (Health Technology Assessment) Statistics group, including HTA submissions.
  • Interacts with multidisciplinary scientists, company subsidiary project leads and Late Development Statisticians to support HTA submissions
  • Designs, develops and evaluates tools for HTA evaluations
  • Gives input to VEST (Value Evidence Sub Team) as statistical representative and may contribute to VEST meetings
  • Primary activities for the position :

  • Leads and provides statistical support to the cross-functional teams preparing HTA submissions
  • Plans and executes independently on the ongoing HTA evaluations, including analysis and interpretation of HTA results.
  • Ensure that project deliverables meet analysis and submission requirements

  • Collaborates with Statistical Programming lead to implement methodologies and ensure high quality deliverables for HTA submissions
  • Leads the preparation of the written reports to effectively communicate results of HTA evaluations to the outcomes research and company affiliate teams
  • Designs, develops and applies HTA methods, processes and standard tools
  • Provides responses for queries from HTA agencies related to statistical analyses and methodological rationale
  • Evaluate appropriateness of available software for planned analyses and ascertains needs for potential program development of novel statistical methodology.
  • Leads research activities for innovative statistical methods and applications in HTA activities
  • Mentors junior staff or contractors in functional activities within a project
  • Qualifications

    Education and Minimum Requirement :

    PhD or equivalent degree in statistics / biostatistics or related discipline with a minimum of 6 years relevant work experience, or Master s with a minimum of 9 years relevant work experience, or bachelor’s with at least 15 years of relevant work experience

    Required Skills and Experience :

  • Good knowledge of biostatistical methodologies and experimental design, including meta-analyses and time to event methodologies.
  • Understanding of data management and clinical concepts applied to drug development within the pharmaceutical industry.

  • Working knowledge of statistical and data processing software e.g. SAS and / or R. Demonstrates strong interest in statistical research activities and in application of novel methods to clinical development.
  • Team oriented, strong collaboration skills and ability to work effectively across cultures.
  • Must also demonstrate the ability to learn, be proactive and motivated, and consistently focus on details and execution.
  • Project management proficiency
  • Strong communication skills, ability to work with staff from different functional background.
  • Preferred Skills and Experience :

  • Strong knowledge of computer systems and clinical databases systems in a statistical environment.
  • Experience in CDISC data standards (SDTM, ADAM)
  • Understanding of biology of disease and drug development.
  • Publication record in peer reviewed statistical / medical journals
  • The BARDS organization has established in Europe its Center of Excellence supporting Health Technology Assessment (HTA) dossiers.

    Our statisticians and statistical programmers collaborate with multiple functional areas across the company and with our local affiliates to ensure that the clinical trial data representing our products is characterized properly in these dossiers, and to develop innovative statistical approaches to novel problems in the HTA space.


    Our company has had a presence in Switzerland since 1963. With a regional office and manufacturing / packaging facility, Lucerne is considered the center of operations.

    Approximately 1,000 people work collaboratively at the four Lucerne locations (Weystrasse, Citybay, Schachen and Kriens).

    A fifth location has been recently established in Zurich, aimed at accelerating the development and commercialization of many of our company’s medicines and vaccines, which supports our mission to save and improve lives around the world.

    The new location has a target date of 2021 for operational readiness.

    We are proud to be certified as a Top Employer Switzerland and Top Employer Europe showing the company’s commitment to our employees and the community around us.


    The recently opened new location in Zurich focuses on accelerating research, data and commercialization of our medicines and vaccines.

    The new office will be staffed by teams working in strategic and operational roles in medical affairs, clinical development, access and marketing operations functions.

    The new location has a target date of 2021 for operational readiness.

    Who we are

    Merck & Co., Inc., Kenilworth, New Jersey, USA is known as Merck in the United States, Canada & Puerto Rico. We are known as MSD in Europe, Middle East, Africa, Latin America & Asia Pacific.

    We are a global biopharmaceutical leader with a diverse portfolio of prescription medicines, oncology, vaccines and animal health products.

    We are driven by our purpose to develop and deliver innovative products that save and improve lives. With 69,000 employees operating in more than 140 countries, we offer state of the art laboratories, plants and offices that are designed to Inspire our employees as we learn, develop and grow in our careers.

    We are proud of our 125 years of service to humanity and continue to be one of the world’s biggest investors in Research & Development.

    What we look for

    In a world of rapid innovation, we seek brave Inventors who want to make an Impact in all aspects of our business, enabling breakthroughs that will affect generations to come.

    We encourage you to bring your disruptive thinking, collaborative spirit and diverse perspective to our organization. Together we will continue Inventing For Life, Impacting Lives while Inspiring Your Career Growth.


    We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment.

    We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

    Search Firm Representatives Please Read Carefully

    Merck & Co., Inc., Kenilworth, NJ, USA, also known as Merck Sharp & Dohme Corp., Kenilworth, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities.

    All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.

    No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place.

    Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

    Employee Status : Regular

    Relocation :

    Domestic / International

    VISA Sponsorship :

    Travel Requirements :

    Flexible Work Arrangements :

    Shift : Not Indicated

    Not Indicated

    Valid Driving License :

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