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VP or SVP, Regulatory Affairs

Location
Watertown, Massachusetts, United States
Compensation
Not disclosed
Level
vp
Type
full time

Posted by employer 3 months ago

First seen on Joblaze 1 week ago

Last verified on the company career page 3 hours ago

Not disclosed in this posting: compensation, years of experience, work arrangement, visa sponsorship.

Joblaze summary

In this role, the VP or SVP of Regulatory Affairs at Acrivon Therapeutics will oversee the development and execution of regulatory strategies to ensure compliance with industry standards. The position requires expertise in regulatory submissions and a strong understanding of the pharmaceutical landscape, particularly in clinical development. This role is ideal for a seasoned professional with a robust background in regulatory affairs, capable of leading teams and influencing cross-functional initiatives. Acrivon is focused on advancing innovative therapies, making this a pivotal position within a dynamic organization.

Joblaze insights

  • Listed 8 days ago on Joblaze — tracked directly from Acrivon Therapeutics's career page.

Quick facts

What seniority level is this role?
Acrivon Therapeutics targets vp candidates for this position.
Is this full-time or contract?
Full-time for this VP or SVP, Regulatory Affairs role at Acrivon Therapeutics.

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