Regulatory
Aclinix Research stands as a trusted partner offering unparalleled global regulatory staffing and recruiting support across every phase of the drug and device development life cycle. Our expertise lies in meticulously identifying Regulatory Affairs talent, honed to excel both within the intricacies of the US regulatory framework and the complexities of global regulatory environments.
Within our talent network, you’ll find seasoned professionals who possess a wealth of experience in managing entire portfolios spanning diverse Therapeutic Areas and Indications. From pharmaceuticals to medical devices, our specialists bring a depth of knowledge and a breadth of skills to navigate regulatory requirements with finesse and precision.
Whether your organization requires immediate support through contract staff augmentation, seeks the flexibility of Functional Service Provider (FSP) solutions, aims for seamless transitions with contract-to-hire arrangements, or prefers direct hire resources, Aclinix Research offers tailored staffing solutions to meet your unique needs.
Our commitment extends beyond merely filling positions; we strive to forge lasting partnerships, providing strategic guidance and unparalleled support to drive your regulatory initiatives forward. With Aclinix Research by your side, you can navigate the ever-evolving regulatory landscape with confidence, knowing that you have a dedicated team of experts focused on your success.
Here's a glimpse of the searches we've supported
- Sr. Director, Regulatory Affairs
- Regulatory Affairs Manager
- Regulatory Affairs Specialist
- Submissions Specialist
- Regulatory eCTD Publisher
- Regulatory Labeling Lead
- Regulatory Ad-Promo
- Regulatory Writers
Our team is adept at sourcing top-tier talent across the following functional domains
- Global Regulatory Strategy
- Regulatory Operations and Submissions
- Labeling/Artwork
- Advertising and Promotions
- Generics/Biosimilars
- Regulatory Intelligence
- Regulatory Compliance Audits
- Regulatory Due Diligence
- Post-Market Regulatory Activities
- Regulatory Training and Education
- Regulatory Agency Interactions
- Regulatory Compliance Remediation
- Regulatory Due Date Management
- Chemistry, Manufacturing, and Controls (CMC) – Strategy / Writing / Operations