
1001 - 5000 employees
Founded 1997
đ§Ź 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.
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1001 - 5000 employees
Founded 1997
đ§Ź 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.
⢠Responsible for the design, analysis, and/or interpretation of clinical studies as a lead ⢠Collaborate with the sponsor, PM, clinical team, data managers, medical writers, statistical programmers, and other team members ⢠Manage the creation, review, maintenance, and oversight of all contracted statistical output and activities ⢠Act as the study lead for multiple studies, clinical programs, and/or large/complex studies ⢠Provide feedback regarding issues or improvements to initial proposed designs ⢠Write summaries of findings and results for interim analyses or final reports ⢠Provide mentoring and support to junior statisticians
⢠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 ⢠Communication skills ⢠Presentation skills ⢠Knowledge of the MS Office Suite ⢠Proficiency in one or more statistical programming language (SAS Preferred). ⢠Collaboration across cross-functional teams ⢠Good understanding of ICH and regulatory landscape. ⢠Knowledge of advanced statistical methods (e.g., survival analysis, logistic regression, and mixed models) ⢠Fluency in English
⢠Collaborative, international team ⢠Work-life balance support ⢠Opportunity to grow careers
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