
1001 - 5000 employees
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
Allucent is a leading partner for small and mid-sized biotech companies, offering innovative regulatory and clinical development solutions. With over 30 years of experience, Allucent specializes in therapeutic expertise, clinical pharmacology, regulatory strategy, drug safety, and the pharmacovigilance processes needed to bring new therapies to market. Their comprehensive services address challenges from early-phase drug discovery through clinical trials and post-marketing surveillance, supporting various therapeutic areas such as oncology, infectious disease, neurology, autoimmune diseases, and rare diseases. Allucent's commitment to fostering breakthrough science helps biotech companies navigate the complexities of drug development efficiently and effectively.
🕒 July 7
Quality Assurance Officer II coordinating quality documentation, audits, and regulatory inspections at Allucent. Leading quality activities and ensuring compliance within the organization.
Google Cloud Platform
🕒 July 6
Project Director overseeing quality and management of clinical trials at Allucent. Leading project teams and ensuring client satisfaction while ensuring compliance with regulatory standards.
🕒 July 1
Senior Clinical Programmer I leading programming activities contributing to successful global clinical studies at Allucent. Ensuring high-quality data and regulatory compliance throughout the study lifecycle.
🗣️🇫🇷 French Required
🕒 June 26
Senior Clinical Programmer I leading clinical programming activities for global studies at Allucent. Collaborating across teams to ensure high-quality data and regulatory compliance in clinical trials.
🕒 June 25
Chief Medical Officer leading Medical Affairs and Pharmacovigilance for innovative global CRO. Responsible for strategy, reporting, client satisfaction, and team management.
🕒 June 24
Local Contact Person for Pharmacovigilance managing compliance with regulations in Poland. Collaborating with regulatory authorities and supporting post-marketing activities for client products.
🕒 June 10
Chief Medical Officer responsible for Medical Affairs and Pharmacovigilance strategy at global CRO Allucent. Leading departmental strategy and overseeing profitability and client satisfaction.
🕒 June 2
Associate Director role in Clinical Pharmacology leading modeling and simulation efforts. Contributing to drug development strategies and regulatory interactions within a dynamic environment.
🕒 June 2
Senior Director, CMC assisting biopharmaceutical companies with clinical trials for drug and device development. Leading CMC strategy from evaluation to regulatory submission and commercial launch.
🕒 May 22
Project Director overseeing clinical study trials in neuroscience, immunology, and infectious diseases. Managing project delivery, client satisfaction, and regulatory compliance for clinical trials.
🕒 May 7
Associate Director responsible for leading modeling and simulation in drug development. Guiding teams and providing strategic insights for regulatory interactions with clients.
🗣️🇫🇷 French Required
🕒 March 31
Statistical Consultant leading biostatistics consulting services for clinical trials at Allucent. Providing expertise in statistical analysis, project management, and client relationships in drug development.