Biostatistisciain

TFS HealthScience; Paris; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading global Contract Research Organization is seeking a Biostatistician in Paris to prepare, conduct, and complete statistical tasks for clinical studies. The ideal candidate will have a Bachelor’s or Master’s in Biostatistics and proficiency in SAS programming. This role offers a competitive compensation package and opportunities for both personal and professional growth in a collaborative environment.

Prestations

Comprehensive benefits

Opportunities for personal and professional growth

Qualifications

• A Bachelor of Science (BSc) or Master’s Degree in related discipline.
• Proficiency in SAS programming.
• Good verbal and communication skills.

Responsabilités

• Responsible for planning, performance, reporting, and documentation of statistical tasks.
• Assist in development of Study Protocols and reports by providing statistical input.
• Write the statistical sections in the Study Protocol.

Connaissances

Proficiency in SAS programming

Good verbal and communication skills

Ability and willingness to travel

Formation

Bachelor of Science (BSc) or Master’s Degree in Biostatistics, Statistics or related discipline

Description du poste

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.

Join Our Team as a Biostatistician

About this role

As part of our Strategic Resourcing Solutions (SRS) team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals.

The Biostatistician is responsible for preparing, conducting and completing statistical tasks in assigned Study Teams, according to company policies, SOP’s and regulatory requirements.

Key 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.

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.

What We Offer

We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients.

A Bit More About Us

Our journey began over 25 years ago in Sweden, in the city of Lund. As a global CRO with the ultimate goal of ensuring patients’ safety and well-being, we provide biotechnology and pharmaceutical companies with tailored clinical development solutions. We currently operate in 17 countries across Europe, North America, Asia Pacific and the Middle East.

Our core values of Trust, Quality, Flexibility and Passion are what make 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 organization.

#Together we make a difference