Biomapas offers comprehensive solutions in clinical research, regulatory affairs, pharmacovigilance, and medical information, providing essential support throughout the clinical trial process to enhance drug development and ensure compliance.
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Biomapas Clinical Operations is hiring a freelance Senior Start Up Associate in Greece to manage country- and site-level clinical study start-up activities under CTR via CTIS and local regulatory requirements.
Biomapas is hiring a Medical/Clinical Safety Specialist to support global pharmacovigilance operations by processing safety cases, maintaining regulatory compliance, and coordinating safety reporting across clinical and local activities.
Pharmacovigilance Specialist (Japanese Speaking) at a global organization, working remotely to support local and global literature screening and ensure compliance with pharmacovigilance and quality requirements.
Associate Director International PV at a pharmacovigilance organization leads the international PV office and oversees global PV operations, compliance, and team performance across EU/UK activities.
Biomapas is seeking a Clinical Research Associate in Ukraine to oversee clinical trials and site operations in a hybrid office/home-based role, ensuring studies are run in compliance with protocol, regulatory requirements, and Good Clinical Practice standards.
