Biostatistician II

Biostatistician II
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life – To enable our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. As part of our clinical research portfolio, our CorEvitas evidence-based solutions specialize in generating data intelligence and clinical insights needed to bring safe and effective treatments to market. Your objectivity and dedication to patient safety will improve health outcomes that people and communities depend on – now and in the future.
A day in the life:
Ensures compliance with the activities outlined in the department's SOPs. 
Follows departmental procedures for statistical analyses and programming work.
Leads a project team. Conducts team meetings, maintains project timelines, 
assesses resources needed, provides resources, and prepares the budget. 
Ensures that SOPs are being followed and that appropriate project 
documentation is ongoing.
Interacts with the sponsor on all aspects of the project.
Coordinates with programmers and data management personnel as to database maintenance, updating and documentation. Provides guidance for database structures for analysis.
Provides sample size calculations and reviews protocols for completeness, 
appropriateness of clinical design, and sound statistical analysis.
Provides randomization schemes and appropriate documentation.
Develops statistical analysis plan, including analysis database and table and 
 
Hiring requirements:
Education:
Master's degree in statistics, biostatistics, mathematics is required.
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. 
Experience:
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years’).
SAS and CDISC are required.
CRO, pharma or closely related industry clinical trial experience is required.
Project lead experience is required.
R programming is preferred.
Knowledge, Skills and Abilities: 
Solid SAS® programming skills (Proficient in BASE, STAT, MACRO and GRAPH) and understanding of database structures
Capable of providing mentorship and promoting teamwork in a multi-disciplinary team setting
Solid understanding of statistical principles and good statistical skills
Capable of creating study specifications and providing support in the review of data management documentation
Good project management skills as shown through management of multiple projects
Solid written and verbal communications skills, including proficiency in the English language
Good organizational skills with the ability to adapt and adjust to changing priorities
Positive attitude and the ability to work well with others
Our Mission is to enable our customers to make the world healthier, cleaner and safer. As one team of 100,000+ colleagues, we share a common set of values – Integrity, Intensity, Innovation, and Involvement – working together to accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need.
Apply today!
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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Required Skills
Required Languages
🇬🇧 English