Biostatistician m/f/d

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, EU 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 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 looking for a
Biostatistician, HTA Statistics
( full-time, indefinite )
to join the team based in our office in Brussels (Belgium).
The BARDS organization has established in Europe its Centre of Excellence supporting Health Technology Assessment (HTA) dossiers with presence in Brussels (Belgium), London (United Kingdom) and Zürich (Switzerland).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.
The primary activities include but are not limited to:
o
Provide statistical support to projects in the BARDS HTA Statistics group, including HTA submissions.
o
Contribute to the design and development of scientific tools for HTA evaluations.
o
Execute on ongoing HTA evaluations, including analysis and interpretation of HTA results.
o
Collaborate with Statistical Programming to implement methodologies and ensure high quality deliverables for HTA submissions.
o
Contribute to the preparation of the written reports to effectively communicate results of HTA evaluations to the Centre for Observational and Real-World Evidence (CORE) and our company’s subsidiary teams.
o
May evaluate appropriateness of available software for planned analyses and ascertains needs for potential program development of novel statistical methodology.
o
May be involved in research activities for innovative statistical methods and applications in HTA activities.
Qualifications:
o
Master’s degree or bachelor’s degree in statistics or a related quantitative field,
o
Fluency in English (oral and written).
o
Good knowledge of biostatistical methodologies and experimental design, including meta-analyses and time to event methodologies.
o
Understanding of data management and clinical concepts applied to drug development within the pharmaceutical industry.
o
Proven knowledge of statistical and data processing software e.g., SAS and/or R.
o
Demonstrates strong interest in statistical research activities and in application of novel methods to clinical development.
o
Team oriented, strong collaboration skills and ability to work effectively across
cultures.
o
Must also demonstrate the ability to learn, be proactive and motivated, and consistently focus on details and execution.
Our Quantitative Sciences team use big data to analyse the safety and efficacy claims of our potential medical breakthroughs. We review the quality and reliability of clinical studies using deep scientific knowledge, statistical analysis and high-quality data to support decision making in clinical trials. As a company, we are committed to 'Inventing for Life' in all that we do. We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. Please don't hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.Please feel free to speak to us about what flexibility means to you during your application or click on the link to find out more about our hybrid working model Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, 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 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, EU 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 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 looking for a
Biostatistician, HTA Statistics
( full-time, indefinite )
to join the team based in our office in Brussels (Belgium).
The BARDS organization has established in Europe its Centre of Excellence supporting Health Technology Assessment (HTA) dossiers with presence in Brussels (Belgium), London (United Kingdom) and Zürich (Switzerland).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.
The primary activities include but are not limited to:
o
Provide statistical support to projects in the BARDS HTA Statistics group, including HTA submissions.
o
Contribute to the design and development of scientific tools for HTA evaluations.
o
Execute on ongoing HTA evaluations, including analysis and interpretation of HTA results.
o
Collaborate with Statistical Programming to implement methodologies and ensure high quality deliverables for HTA submissions.
o
Contribute to the preparation of the written reports to effectively communicate results of HTA evaluations to the Centre for Observational and Real-World Evidence (CORE) and our company’s subsidiary teams.
o
May evaluate appropriateness of available software for planned analyses and ascertains needs for potential program development of novel statistical methodology.
o
May be involved in research activities for innovative statistical methods and applications in HTA activities.
Qualifications:
o
Master’s degree or bachelor’s degree in statistics or a related quantitative field,
o
Fluency in English (oral and written).
o
Good knowledge of biostatistical methodologies and experimental design, including meta-analyses and time to event methodologies.
o
Understanding of data management and clinical concepts applied to drug development within the pharmaceutical industry.
o
Proven knowledge of statistical and data processing software e.g., SAS and/or R.
o
Demonstrates strong interest in statistical research activities and in application of novel methods to clinical development.
o
Team oriented, strong collaboration skills and ability to work effectively across
cultures.
o
Must also demonstrate the ability to learn, be proactive and motivated, and consistently focus on details and execution.
Our Quantitative Sciences team use big data to analyse the safety and efficacy claims of our potential medical breakthroughs. We review the quality and reliability of clinical studies using deep scientific knowledge, statistical analysis and high-quality data to support decision making in clinical trials. As a company, we are committed to 'Inventing for Life' in all that we do. We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. Please don't hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.Please feel free to speak to us about what flexibility means to you during your application or click on the link to find out more about our hybrid working model Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, 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:RegularRelocation:VISA Sponsorship: Travel Requirements: Flexible Work Arrangements:HybridShift:Valid Driving License:Hazardous Material(s): Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.
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