ERGOMED
1001 - 5000 employees
Founded 1997
𧏠Biotechnology
đ Pharmaceuticals
âď¸ Healthcare Insurance
Biotechnology ⢠Pharmaceuticals ⢠Healthcare Insurance
ERGOMED is a global group providing specialized services to the biotechnology and pharmaceutical industries. It operates under different service lines, including Ergomed Clinical Research, PrimeVigilance, and ADAMAS Consulting, and is dedicated to providing full-service clinical research organization (CRO) capabilities. Focused on oncology, rare diseases, and complex trials, it also offers end-to-end pharmacovigilance and medical information services, as well as comprehensive GxP audits. Ergomed is committed to supporting drug development with a global presence in around 100 countries.
Principal Biostatistician
đĽ 1 minute ago
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ERGOMED
1001 - 5000 employees
Founded 1997
𧏠Biotechnology
đ Pharmaceuticals
âď¸ Healthcare Insurance
Biotechnology ⢠Pharmaceuticals ⢠Healthcare Insurance
ERGOMED is a global group providing specialized services to the biotechnology and pharmaceutical industries. It operates under different service lines, including Ergomed Clinical Research, PrimeVigilance, and ADAMAS Consulting, and is dedicated to providing full-service clinical research organization (CRO) capabilities. Focused on oncology, rare diseases, and complex trials, it also offers end-to-end pharmacovigilance and medical information services, as well as comprehensive GxP audits. Ergomed is committed to supporting drug development with a global presence in around 100 countries.
đ Description
⢠Act as the study lead for multiple studies, clinical programs, and/or large/complex studies with responsibility for all biostatistics related activities ⢠Support the review and development of clinical programs ⢠Ensure work is performed on time ⢠Provide review and oversight to statistical output ⢠Write summaries of findings and results to be included as part of study reports
đŻ Requirements
⢠Masterâs degree (or Higher) in biostatistics, statistics, mathematics or other related disciplines ⢠General understanding and application of biostatistics in clinical trials ⢠Strong previous related experience working in a Contract Research Organization ⢠Knowledge of the MS Office Suite ⢠Proficiency in one or more statistical programming language (SAS Preferred) ⢠Good understanding of ICH and regulatory landscape ⢠Knowledge of advanced statistical methods (e.g., survival analysis, logistic regression, and mixed models) ⢠Fluency in English
đď¸ Benefits
⢠Collaborative international team ⢠Work-life balance ⢠Opportunity for growth ⢠Meaningful work on complex trials ⢠Commitment to integrity and trust
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