Principal Statistician - EMEA - Sponsor-dedicated
Syneos Health
Amsterdam, North Holland, Netherlands
Remote
Expert
posted 4 days ago
Vacancy Summary
Join Syneos Health as a Principal Statistician, where you'll leverage your expertise in statistical analysis to support clinical trials across EMEA. Collaborate with a dedicated team to drive impactful solutions in drug development and commercialization.
Syneos Health® is a leading fully-integrated life sciences services organization dedicated to accelerating customer success. We partner with innovators throughout the drug development and commercialization continuum, helping them navigate complexity and accelerate progress.
Our Clinical Solutions team embodies a drug development mindset, utilizing extensive experience and deep expertise to understand customer needs and shape effective solutions.
In this role, you will serve as a key resource in the statistical department, mentoring biostatisticians and overseeing training plans for associates. You will direct activities on assigned projects to ensure timely, high-quality work and provide independent reviews of project outputs. Your responsibilities will include:
At Syneos Health, we are committed to developing our people through career progression, training, and a supportive culture. We strive to create an inclusive environment where everyone can be their authentic selves. Discover how we are shaping the future of healthcare and driving impact for our customers.
Additional Information: Tasks and responsibilities listed are not exhaustive. The company may assign other duties as needed. Equivalent experience and qualifications will be considered. This posting does not constitute an employment contract. We are committed to compliance with the Americans with Disabilities Act and providing reasonable accommodations as necessary.
Required skills
Quality Control
Compliance
Verification
Alignment
Customer Success
monitoring
Driving
Communication Skills
Design
Quality Work
English
regulatory submissions
SAS
Healthcare
Commercialization
Clinical Trials
Statistical Analysis
Proposals
ACT
CAN
Regulatory Guidelines
Training
Management
Board
data
mentoring
specifications
CSR
Culture
Drug Development
R Programming
SAP
Safety
Clinical Study Reports
Discipline
Progress
English level
Fluent
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