Sr. Regulatory Affairs Associate
WEP Clinical (3 months ago)
About this role
The Sr. Regulatory Affairs Associate at WEP Clinical supports and executes regulatory strategies for global access programs and clinical trials, enabling timely access to medicines for patients with unmet medical needs. The role serves as a primary regulatory contact across regions, working closely with internal teams, clinical sites, and health authorities. It is positioned within a mission-driven organization focused on early access to medicines and clinical research support services. The position emphasizes collaboration, innovation, and contribution to organizational compliance and efficiency within Regulatory Affairs.
Required Skills
- Regulatory Strategy
- Regulatory Submissions
- Regulatory Compliance
- Global Regulations
- Clinical Trials
- Expanded Access
- Compassionate Use
- Named Patient Programs
- Stakeholder Communication
- Cross Functional Collaboration
+15 more
Qualifications
- Bachelor's Degree
About WEP Clinical
wepclinical.comWEP Clinical is a full-service, "Complete CRO" built for biotech sponsors, offering bespoke services across the full lifecycle of drug development. They deliver clinical trial management (Phase I–IV) and complementary Treatment Access, Market Access and Commercialization solutions to help sponsors advance medicines and reach patients worldwide. With a proven track record supporting 60+ clinical programs globally, WEP focuses on tailored strategies to accelerate development, access and launch.
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