PANDA LIFE SCIENCES is a specialist recruitment agency dedicated to placing high-level candidates in permanent and freelance roles within the Pharmaceutical, Medical Device, Biotech and Food sectors across Europe. By working closely with candidates and clients in meeting challenging business demands, the Panda team have developed an extensive client base consisting of the world’s leading Life Sciences organizations. As simple as it sounds, we believe that a sustainable recruitment business model is based on long-term relationships, something we take pride in.
We are looking for an interim Regulatory Affairs Project Manager for one of our clients in the Antwerp region for a period of 1 year!
Responsible for the Global Regulatory Team support and you will represent the regulatory program management at the Global Regulatory Team.
Coordination of the maintenance, creation, management and timely submission of regulatory project budgets
Managing the regulatory development plan
Translates the regulatory strategy into realistic and executable regulatory deliverables with clear assumptions based on GRT input
Close collaboration with the compound development team for alignment of the RA strategy and compound development strategy
Work close with other program managers in terms of functional and regulatory strategy
Support of early risk identification and development of mitigation strategies
You will be the point of contact for Regulatory Program Management activities
Master or Bachelor Degree
Minimum of 5 years Regulatory experience
Experience in the Pharmaceutical or Biotech industry is preferred
Preferred experience in: Oncology, Immunology, Neuroscience, Infectious Diseases and Vaccines, or Cardiovascular/Metabolism
Experience in project management and change management. Be flexible and creative in a changing and improving working environment.
Effective experience in handling of conflicting priorities in changing cross-departmental is required
Good written and verbal skills in English
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