Hobson Prior is seeking a Director of Regulatory Affairs to support regulatory activities for products in development. The successful candidate will play a key role in guiding regulatory strategies and ensuring compliance with health authority requirements.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
- Provide support for regulatory activities in the US.
- Lead regulatory efforts for clinical development programs.
- Offer advice on regulatory strategies and plans.
- Collaborate with the team to prepare and submit documents to health authorities.
- Act as the main contact with health authorities.
- Participate in team meetings to advise on regulatory strategies and submission processes.
Key Skills and Requirements:
- Degree in a scientific field.
- Experience in US regulatory affairs within the pharmaceutical or biotechnology industry.
- Familiarity with regulatory submissions in various areas.
- Experience in oncology is beneficial.
- Strong attention to detail and ability to communicate complex information clearly.
For more information, please contact Henry LeLacheur.
Apply now
If you are interested in learning more or applying to this exciting opportunity then please click 'Apply' and upload a copy of your CV. Alternatively for further details or to talk directly to a life sciences recruitment specialist directly please select 'Contact me' at the top of this page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
By providing your details and submitting this form you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.
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