We are seeking candidates with experience leading multi-site clinical trials for implantable neuromodulation devices to join our team as Head of Clinical and Regulatory Affairs.
This role is responsible for overseeing Motif’s clinical department and functions including Clinical Affairs, Clinical Operations, Clinical Science, and Regulatory Affairs. Within Clinical Operations specifically, you will be responsible for running our clinical trials from end-to-end. You will partner closely with Leadership, Quality, R&D, Operations, and Marketing teams, in service of a technology with the potential to change how mental health is treated.
If you have a passion for building elite clinical execution inside a startup environment, apply now to be part of our dedicated team.
Job Location: Remote (Houston, Texas preferred)
Does this sound like you?
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You’ve run a multi-site clinical trial for an implantable neuromodulation device and know exactly what can go wrong… and how to avoid it!
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You enjoy cross-functional coordination to stitch together clinical evidence generation, clinical execution, and regulatory necessities.
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You want to build a scalable clinical function that plans and manages its own work, rather than one that depends on you for every decision.
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You thrive with direct strategic communication with leadership helping to ensure all the pieces work together.
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You are excited by the opportunity to represent Motif at industry podiums and with KOLs, but you’re just as comfortable personally chasing down a site activation delay.
If yes to the above, then you may love working with Motif as it is being built by highly dedicated people with passion for neurotechnology, clinical product development, and putting the patient first. We are looking for people with the same energy who will thrive in a high growth, high autonomy environment.