Executive Regulatory Affairs Consultant – Precision Medicine / Digital Health
Location : Fully Remote – Europe or USA
Contract length : 6 months initially (likely extension to 12+ months)
Key responsibilities
- Provide regulatory input and support for precision medicine / digital health submissions and processes
- Collaborate closely with cross-functional teams across Europe and the US
- Review, prepare and coordinate regulatory documentation
- Ensure compliance with relevant EU and global regulations, guidance and standards
- Contribute to shaping regulatory strategy while maintaining a pragmatic, delivery-focused approach
- Strong regulatory affairs experience within pharma / biotech, ideally with exposure to precision medicine, biomarkers, or digital health solutions
- EU regulatory experience preferred; US regulatory knowledge also valued
- Pragmatic, solution-oriented mindset with ability to balance strategy and execution
- Collaborative team player with excellent communication skills
- Able to work independently in a fully remote setting
- Start : ASAP
- Contract length : 6 months (extension very likely to 12+ months)
How to Apply
Interested? Send your CV directly to
Please note : Only candidates matching the criteria above will be contacted. Due to high volumes, if you don’t hear back within 10 days, consider your application unsuccessful.
About Elemed
Elemed is an equal opportunity employer. We celebrate diversity and foster an inclusive environment for all candidates and contractors.
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