This is what you will do:
The Associate Regulatory Affairs Director (ARAD), Regulatory Science & Execution will be responsible for supporting strategies and executing regulatory activities for assigned product and regulatory jurisdictions, with the intention of achieving successful registration and lifecycle management of unique and technologically complex products serving patients with rare diseases and unmet medical needs.
This individual will, with a high sense of urgency, provide operational and strategic regulatory input to cross-functional teams responsible for executing programs in relevant regulatory jurisdictions. The individual will also ensure effective communication and constructive working relationships with business partners and representatives of regulatory authorities.
You will be responsible for:
Job Duties and Responsibilities
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