Lead regulatory activities and team management while assisting biopharmaceutical clients with drug, biologic, or medical device regulatory submissions.
At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.
We are looking for a Vice President of Regulatory Affairs to join our A-team (hybrid*/remote). As a VP Regulatory Affairs at Allucent, you are responsible for assisting clients with the regulatory activities of drug, biologic or medical device product.
About the role
As the VP Regulatory Affairs, you will:
This role is open to considering candidates from United States, Canada, Countries within the EU, and United Kingdom.
Requirements
Skills:
Benefits
Benefits of working at Allucent include:
Disclaimers:
*Our office-based work policy encourages a dynamic work environment, prescribing a minimum of 2 days in office per week for employees within reasonable distance from one of our global offices.
“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”
#LI-Remote #LI-Hybrid #LI-TCW
Education Stipend
Departmental Study/Training Budget for furthering professional development
Flexible Work Hours
Flexible Working hours (within reason)
Allucent helps small to medium biopharmaceutical companies navigate the complexities of clinical trials, ensuring they can bring innovative therapies to patients around the world. Our focus on efficiency and partnership enables us to streamline the development process for life-changing treatments.
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