Senior CMC Data Analyst

Global Responsibility Support CMC Specialists within the R&D department by taking responsibility for managing analytical methods used in protein characterisation at internal and external labs, with specific focus on bio-functional/immunological/potency assays (cell based assays, binding assays including ELISA, MSD, SPR…). The senior CMC Data Analyst will assist assays development at 3rd parties labs, plan and… Read more »

Medical Advisor

Global Responsibility Define, develop and control execution of the clinical drug development strategy and the clinical evaluation strategy, together with the scientific leadership of the commercial activities. Specific Responsibilities Lead clinical strategic global development plans through the execution and management of the biosimilar clinical trials, assuming the overall management of the clinical trials. Contribute to… Read more »

International Regulatory Affairs Specialist

Global Responsibility: Will be Responsible for the implementation of regulatory strategies through coordination and preparation of submission documents for the registration of the Biotech products in international markets (including EU, MENA, LATAM, North Africa, Asia).Ensure timely registration of products in compliance with applicable regulation and guidelines. Main Requirements: Bachelor’s degree or equivalent work experience, preferably… Read more »

Clinical Study Coordinator

Global Responsibility: Supervise the proper execution of each part of the study, solving the problems that may arise during its development and taking technical decisions which will be agreed with the superior when they have a significant impact on the cost, timing or outcome of the project, to ensure they comply with the planned time… Read more »