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
Clinical Research Associate (Contractor) Israel
At least 5 years’ experience, strong understanding of ICH-GCP, and comfortable working independently
Sr Pharmacometrician (Europe)
4+ years of relevant work experience, strong analytical skills and strategic thinking
Associate Director, CMC (Central/Eastern Europe)
B.S., R.Ph., M.S., or Ph.D. degree in a scientific area, with 10+ years' relevant experience in drug, biologic, or device development
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
Associate Director, CMC (Central/Eastern Europe)
Requires B.S., R.Ph., M.S., Ph.D., or equivalent degree in scientific area, ≥ 10 years of directly relevant experience, and strong written and verbal communication skills in English
Associate Director, CMC (Central/Eastern Europe)
Requires a B.S., R.Ph., M.S., Ph.D., or equivalent degree, scientific and regulatory knowledge of drug, biologic, or device development, critical thinking and analytical skills, and strong written and verbal communication skills in English
Associate Director, CMC (Central/Eastern Europe)
B.S., R.Ph., M.S., Ph.D. or equivalent degree and ≥10 years' post-degree of directly relevant experience in drug, biologic, or device development
Local Contact Person Pharmacovigilance (LCPPV) - Freelance - PT Poland
University degree, 2+ years of experience in pharmacovigilance, fluency in English
Associate Director, CMC (Central/Eastern Europe)
10+ years of experience in drug, biologic, or device development
VP Regulatory Affairs
B.Sc., M.Sc., Ph.D., or equivalent degree in a scientific area, advanced regulatory knowledge, RAC credentials preferred
+18 More Jobs Available!
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