Alpha Clinical Development is seeking an experienced and dynamic professional to join our team as an Associate Director or Director of Regulatory Affairs. This is a remote role based on the Pacific Side of the USA, offering you the flexibility to make a significant impact in the regulatory landscape of clinical development. If you’re passionate about advancing healthcare through regulatory expertise, we’d love to hear from you!
Why Alpha Clinical Development?
At Alpha Clinical Development, we’re dedicated to driving innovation in clinical research:
- Work remotely from the Pacific Side of the USA
- Contribute to cutting-edge regulatory strategies in a growing field
- Collaborate with a team committed to improving patient outcomes
Job Opportunity
Position
Associate Director / Director of Regulatory Affairs
Location
Pacific Side, USA (Remote Role)
Qualifications
- Master’s degree in Life Sciences or a related field (required)
- PhD or advanced degree (preferred)
Experience
- 8–12+ years in regulatory affairs
- Strong expertise in FDA submissions (BLA, NDA, and other filings)
- Oncology experience (highly desirable)
Key Skills
- Ability to interact effectively with the FDA and other health authorities
- Proven track record in managing complex regulatory filings
How to Apply
Ready to take the next step? Send your resume to:
- Email: rafia.ishfaq@acdlimited.com
Please include “Associate Director/Director Regulatory Affairs” in the subject line.
Shape the Future of Clinical Development
This is your chance to lead regulatory efforts at Alpha Clinical Development, leveraging your expertise to navigate FDA processes and advance oncology solutions. If you meet the qualifications and thrive in a remote, high-impact role, apply today and join our mission to transform healthcare!
For questions, feel free to reach out via email. We’re excited to connect with talented regulatory professionals like you!
