Senior Consultant/ Principal Consultant Biostatistics (Advanced Analytics)
United Kingdom, Remote Additional Locations: , Slovakia; Bucharest, Bucureşti, Romania; Dublin, Dublin, Ireland; Madrid, Madrid, Spain; Milan, Milano, Italy; Prague, Czechia; Vilnius, Lithuania; Warsaw, Poland Job ID R0000009934 Category Regulatory / ConsultingAbout this Role
Our Advanced Analytics team is expanding and we are recruiting for a Senior Consultant or Principal Consultant Biostatistician. We are looking lead for experienced lead biostatisticians with familiarity with primary observational data studies. Working knowledge of CDISC standards and R will be a plus.
Position Overview
You will work independently in reviewing protocols, developing SAPs (including mock shells), developing data specifications per CDISC standards, programming and quality control of derived datasets and statistical outputs, production of reports, and providing statistical advice to study teams and clients.
Objectives of the role will include:
Acting as Lead Biostatistician to interact with the study team and the sponsor
Drafting statistical sections of protocols, performing sample size and power calculation for studies, and creating randomization schedules per study design and relevant specifications
Reviewing case report forms (CRFs), data management plans, data specifications, and other related study documents
Independently developing statistical analysis plans
Preparing specifications for CDISC and other analysis datasets
Independently developing SAS programs to generate listings, tables and figures as outlined by a statistical analysis plan
Performing QC of TLFs, CDISC and other analysis datasets
Reviewing study protocols and providing input to statistics section
Providing statistical input to Clinical Trial Reports
Aiding business development with statistical considerations for new study bids, preparing biostatistics budgets, and attending bid defense meetings
Serving as a mentor to junior-level biostatisticians to help develop skills
Qualifications
Expertise in primary observational studies
Strong basis in fundamental statistical concepts and methods and familiarity with techniques such as performing sample size and power calculation for studies, and creating randomization schedule per study design and relevant specifications
Familiarity with specifications for CDISC and other analysis datasets
Strong statistical programming skills with standard software, including SAS and R
Strong communication (spoken and written) and problem-solving skills, and an ability to learn quickly
Ability to communicate effectively, in non-technical terms, with project team members
Ability to work well in a team as well as independently and take leadership roles with regard to methodological elements in projects
Education and Experience
Master's or Doctoral Degree in Statistics, Biostatics, Mathematics, Data Science or other quantitative fields.
Language Skills
Competent in written and spoken English
Computer Skills
SAS (Base, Stat, Graph, Macro) and R
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