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Clinical Regulatory Affairs Consultant - Schweiz - NonStop Consulting
Beschreibung
Join a Leading Edge in Pharmaceuticals: Seeking Regulatory Affairs ConsultantOur client is a start up pharmaceutical company actively seeking a seasoned and experience Regulatory Affairs Consultant in Switzerland.
This is going to be a challenging but rewarding position where you will be managing strategy from Phase - product approval.
For this position it will be crucial that you come with experience in a start-up or small company.What We're Looking For:
Clinical Strategy Expertise:
Proven hands-on experience in managing clinical strategies, with a strong focus on FDA and EMEA regulations
Start-Up Experience:
Demonstrated ability to thrive in dynamic start-up environments, bringing agility, innovation, and proactive problem-solving to the table
Regulatory Acumen:
In-depth knowledge of regulatory frameworks and the ability to navigate complex regulatory landscapes seamlessly
Key Responsibilities:
Lead regulatory strategy development and implementation for clinical trials and product approvals. Interface with regulatory agencies, ensuring compliance and advocating for the company's strategic goals. Collaborate with cross-functional teams to align regulatory activities with overall business objectives. Drive continuous improvement in regulatory processes and systems to enhance efficiency and compliance.
