Description
Syneos Health is a leading, fully integrated organisation specialising in life sciences services, designed to accelerate client success. We collaborate with innovators at every stage of the development and commercialisation continuum, helping them navigate complexity, anticipate change, and accelerate progress.
The Regulatory Affairs Associate I will provide regional expertise and lead regulatory submissions for client projects.
Job Responsibilities
- Provide regulatory consultation for internal clinical projects or standalone regulatory projects
- Maintain current knowledge of regulatory guidelines and regulations, including those related to submissions
- Compile, present, and maintain regulatory submissions
- Act as a liaison between regulatory agencies and external clients
- Interact with external regulatory groups and agencies
- Identify the need to analyse relevant regulatory guidelines and regulations, participate in analysis, and communicate results
- Provide regulatory strategy information to project teams and external clients
Qualification Requirements
- Bachelor's degree, preferably in Life Sciences
- Excellent communication, presentation, and interpersonal skills, both written and verbal, with the ability to inform, influence, convince, and persuade
What We Offer
Syneos Health offers opportunities for career growth, training, and recognition, as well as a comprehensive benefits package.