Lead Biostatistician FSP Europe

Work Schedule

Environmental Conditions

Job Description

At Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling 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. With clinical trials conducted in 100 countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio our work spans laboratory digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the future.

We are looking for a lead biostatistician to join the team of biostatistics as part of Quantitative Sciences. The position can be based anywhere in EMEA but preference would ideally be in Belgium. Remote working is possible.

Our client a global mid-sized biotech company focuses on developing innovative treatments for patients with autoimmune diseases. This fast-growing international organization has a strong scientific foundation. If youre looking for a place where your work in partnership with others can have real impactand where youre encouraged challenge yourself and contribute to breakthrough solutions the Lead Biostatistician could be a great fit.

Your role:

• You contribute with your statistical expertise to the design and analysis of one or more clinical trials or the clinical development plan of one compound/program.

• You will closely collaborate with program partners and stakeholders to deliver on the statistical deliverables for one or more clinical trials and contribute to HA submissions

• You will report to a franchise team leader within the Biostatistics and Statistical Modelling organisation

• You will carry out functional responsibilities in accordance with applicable company guidelines and regulatory requirements

Desired Skills Qualifications and Experience:

• You have a master or doctorate (Ph.D.) degree in Statistics or related field with a minimum of 5 years experience (which may include doctoral research in field of biostatistics)

• You have expertise in drug development with a demonstrated track record of advanced knowledge of biostatistics and strong command of its application to clinical trials

• Submission studies support experience required.

• Demonstrates ability to plan supervise implement and monitor the statistical processes for multiple clinical trials

• You are proficient in statistical software (SAS and/or R);

• You are able to collaborate with program partners and stakeholders to deliver on the statistical deliverables for one or more clinical trials

• You can clearly explain complex statistical concepts in written and spoken English

• You are a team-player with focused attitude

• You are able to work autonomously as part of a cross-disciplinary team in a dynamic surrounding of a fast growing biotech company with challenging timelines

What we offer:

• Member of a cross-disciplinary team involved in clinical development of therapeutic antibodies

• A work-environment in a human-sized dynamic rapidly growing biotech company

• Next to a competitive salary with extensive benefits we offer you the chance to grow and be a part of a team driven by creativity innovation and science.

Thermo Fisher Scientific offers employment with an innovative forward-thinking organization and outstanding career and development prospects. We offer an exciting company culture that stands for integrity intensity involvement and innovation!