Labcorp Principal Biostatistician, home-based EMEA in Muenster, Germany
Principal Biostatistician, home-based EMEA
As an experienced Principal Biostatistician in our Late Phase (IIb-III-IV) multi-sponsor business unit, you are central to the successful delivery of complex clinical trials for renowned, innovative and global top pharmaceutical and biotech companies. You will have the opportunity to lead studies through various phases of the clinical development plan and support submissions, regulatory questions, publications as well as ad hoc and post hoc requests.
In this role you will develop and review Statistical Analysis Plans for data presentation, analyses, and provide programming support to your multidisciplinary global project team.
This position allows you to participate in the development of innovative new benchmark drugs for a wide variety of therapeutic areas such as oncology, cardiovascular, respiratory, neurological, diabetes, rare diseases, pain, immunology etc. Your expertise and your work as a Biostatistician has a direct impact on improving the health and lives of thousands of patients around the globe every day. Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers!
What else can you expect from us?
Rewarding and meaningful work in an established, diverse, highly profitable and respected global company
Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.
A genuine work life balance
Flexibility in working hours
A thorough onboarding with support from your personal mentor
A permanent employment contract with Labcorp Drug Development
Excellent training and career development opportunities, as well as support with advancing your individual education
Strong support from your Labcorp Line Manager and your team, as well as from more than 20,000 colleagues worldwide
Lead complex studies such as New Drug Applications submissions or complex, multi-protocol programs, potentially coordinating activities across multiple locations, providing statistical oversight and attending relevant project meetings
Perform project management activities for identified projects including resource planning, timelines and milestone management
Lead the development of complex Statistical Analysis Plans, perform senior review of statistical analysis plans developed by other statisticians
Conduct overall statistical review of Tables Figures and Listings for complex studies prior to client delivery
Review Case Report Form and other study specific specifications and plans
Develop the statistical sections of the protocol for complex studies under the supervision of a statistical consultant
Preparation and review of randomization specifications and generation of randomization schedules
Provide mentoring and training to less experienced staff; provide direction and review work of departmental employees to ensure accuracy and adherence to pertinent departmental policies, practices, and procedures
Present and share knowledge at monthly seminars and/or team meetings and at external scientific meetings and conferences
Attend bid defense meetings for complex studies
Act as Subject Matter Expert and develop or review procedural documents, or work on new initiatives
Represent the department during audits.
Degree in a relevant field such as statistics, computer sciences, etc.
Solid experience of working as a Lead Biostatistician in either a biotech, CRO or pharmaceutical company
Ability to program in one or more statistical software packages (SAS®) used to conduct statistical analyses; SAS proficiency including use of a variety of statistical procedures e.g., non-parametric analysis, linear and non-linear models, categorical data and survival analysis
Proven professional experience with SDTMs, ADaM datasets and TFLs
Proven ability to effectively communicate statistical concepts
A good knowledge of the overall clinical trial process
Competence in the preparation of Statistical Analysis Plans, analysis, reporting, etc. across a variety of trials
Strong organizational skills, an autonomous and collaborative work style, a curious mind and a keen attention to detail
Business fluency in English – both verbal and written – is a must
As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for the chemical testing and crop protection industries.
Labcorp Drug Development is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Our unique perspectives are based on decades of scientific, medical and regulatory expertise.
Did you know?
In July 2022, Labcorp announced its intention to spin off its clinical development business as a separate public company, subject to the satisfaction of certain customary conditions. Fortrea will become the new brand identity for our Clinical Development business in connection with the spin-off, which is expected in mid-2023.
We believe that the exceptional is possible when you have the right partner, so we are looking for the right people to help build a transformative force in Clinical Development. www.fortrea.com
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
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