Biostatistician
hace 4 semanas
Overview:
TFS HealthScience is excited to be expanding our
**Biostatistic **team and we are looking for an experienced, highly motivated
**Senior Biostatistician** who shares our vision of providing clinical research excellence. Our
**Biostatistic** team is a highly experienced international group of professionals led by an industry expert.
We are a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. We combine the full-service capabilities and global reach of a large CRO with the flexibility and personal approach only a mid-size CRO can deliver.
Our cores values of Trust, Quality, Flexibility and Passion are what makes TFS Healthscience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organisation.
**Together we make a difference.**
TFS HealthScience is looking for a
**Senior Biostatistician, home based **in
** Europe.**
The Senior Biostatistician is part of the Global Biometrics Department within Clinical Development
and will work operationally on preparing, conducting and completing Statistical tasks in assigned
Study Teams, according to company policies, SOP’s and regulatory requirements.
The Senior Biostatistician should take the full statistical responsibility for all essential job functions and support other Biostatisticians in their role.
**What can we offer you?**
A great place to work where you will get the chance to push your career to the next level, global environment with global opportunities. You will also get the opportunity to be part of a team with highly intelligent, passionate experts from all over the world. TFS is a place for inspiration where we focus on the patients, saving lives and aiming to increase their quality of life by supporting our clients.
**Responsibilities**:
- As a member of the Study Team, responsible for the planning, performance, report and documentation of statistical tasks during the study process.
- Assist in the development of Study Protocols, CRFs and reports/manuscripts by providing statistical input
- Write the statistical sections in the Study Protocol
- Review the Study Protocol
- Review the CRF to ensure that the design and structure of the CRF meets the specific statistical requirements defined in the study protocol
- Assist in performing/Review sample size calculations
- Define randomisation procedures and producing randomisation lists
- Define appropriate methods for statistical analysis
- Write the Statistical Analysis Plan
- Design the Data Presentation Plan
- Plan and perform statistical analysis (interim and/or final) in accordance with the Study Protocol and the statistical analysis plan
- Validation of the defined statistical methods (by e g goodness-of-fit tests or model checking)
- Perform programming of statistical analyses and study output
- Document and validate programmes and files for analysis
- Manage clinical data to ensure security and confidentiality
- Produce statistical reports
- Assist in writing/reviewing the statistical sections in the study report
- Contact with clients in questions regarding statistical issues in projects
- Actively contribute to the organization and development of routines to enhance the work at TFS
- May provide input into proposals which include Statistics
- File/archive essential documents
Qualifications:
- A Bachelor of Science (BSc) or Master’s Degree in Biostatistics, Statistics or related discipline
- Proficiency in SAS programming
- Good verbal and communication skills - Ability and willingness to travel on occasion
- TFS HealthScience collects and processes personal data in accordance with applicable data protection laws. If you are a European Job Applicant see the _
- privacy notice_
- for further details._
- TFS HealthScience does not discriminate on the basis of race, sex, color, religion, age, national origin, marital status, disability, veteran status, genetic information, sexual orientation, gender identity or any other reason prohibited by law in provision of employment opportunities and benefits._
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