Allucent is on a mission to help bring new therapies to light by solving the distinct challenges of small and mid-sized biotech companies. The company is purpose-built through the convergence of leading providers to address this unmet need. Today, Allucent is a global provider of comprehensive drug development solutions, including consulting, clinical operations, biometrics and clinical pharmacology across a variety of therapeutic areas. With more than 30 years of experience in over 60 countries, Allucent’s individualized partnership approach provides experience-driven insights and expertise to assist its clients in successfully navigating the complexities of delivering novel treatments to patients.
Open Positions
Directeur Adjoint/Dir. Pharmacométricien (AD/Dir. Pharmacometrician)
6-10 years of experience in drug development, pharmacometrics, and regulatory experience
Clinical Data Manager -III
3-5 years of experience in clinical data management with a degree in a relevant field
Sr. Clinical Research Associate (Germany)
Experience in CRA role, understanding of ICH-GCP, and good communication skills
Clinical Research Associate (Contractor) Australia
5+ years of experience as a CRA, strong understanding of ICH-GCP and regulatory guidelines, and ability to communicate in English
Sr. Clinical Research Associate (Germany)
Experience as a CRA, strong understanding of regulatory guidelines, and clear communication skills
Clinical Data Manager III (India)
Life science graduate or equivalent qualification and 6+ years of experience in clinical data management
Local Contact Person Pharmacovigilance (LCPPV) - Freelance - PT Poland
University degree and 2 years of experience in pharmacovigilance post-marketing activities, with up-to-date knowledge of regulatory requirements
Director/Sr. Director, Biostatistical Consulting
15 years of relevant work experience, Master’s degree in a relevant discipline, strong experience in Bayesian designs specifically in oncology studies
Local Contact Person Pharmacovigilance (LCPPV) - Freelance - PT Poland
University degree, 2+ years of experience in pharmacovigilance, fluency in English
VP Regulatory Affairs
B.Sc., M.Sc., Ph.D., or equivalent degree in a scientific area, and equivalent combination of relevant experience in drug, biologic, or device development, with advanced regulatory knowledge of drug, biologic, or device development focusing on regulatory requirements for US, EU/UK, and Canada
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