Clinical Trials Statistician

hace 2 semanas


Ourense, Orense, España beBee Careers A tiempo completo
About This Opportunity

We are currently seeking a highly skilled Principal Biostatistician to join our team. The ideal candidate will have a strong background in statistics and biostatistics, as well as extensive experience working in clinical research. Key responsibilities include serving as the responsible biostatistician on clinical trials, contributing to clinical study protocols, and developing Statistical Analysis Plans.

The successful candidate will be a self-motivated individual with excellent leadership and communication skills. They will also possess a thorough understanding of CDISC standards and regulatory requirements, as well as experience working with Phase 2 and 3 studies. Proficiency in R programming, ESTIMANDS, adaptive designs, and writing SAPs is essential.

In addition to technical skills, the ideal candidate will have strong analytical and problem-solving abilities, as well as the ability to work effectively in a team environment. A Ph.D. in statistics, biostatistics, or a related field with 5+ years of experience in CRO or pharmaceutical companies is required. Alternatively, a Master's degree with 10+ years of experience may also be considered.

\What You Will Do
  • As a Principal Biostatistician, you will be responsible for leading the biostatistical aspects of clinical trials.
  • You will develop and implement Statistical Analysis Plans and ensure compliance with CDISC standards and regulatory requirements.
  • You will also oversee the development of clinical study reports and contribute to press releases and scientific publications.
\Your Qualifications

To be successful in this role, you will need to possess a strong foundation in statistics and biostatistics, as well as significant experience working in clinical research. You will also need to have excellent leadership and communication skills, as well as a strong understanding of CDISC standards and regulatory requirements.

A Ph.D. in statistics, biostatistics, or a related field with 5+ years of experience in CRO or pharmaceutical companies is required. Alternatively, a Master's degree with 10+ years of experience may also be considered.

\Why Choose Us?

We are a world-leading provider of outsourced development and commercialisation services to the pharmaceutical and biotechnology industries. Our team of experts has a proven track record of delivering high-quality results in a timely and cost-effective manner.

We offer a comprehensive reward package, including competitive pay, variable incentives, and employee benefits. We are committed to continuous learning and professional development, and we offer opportunities for career advancement and growth.


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