Regulatory Affairs Associate - CONSULTANT
ClinChoice(1 month ago)
About this role
A Regulatory Affairs Associate Consultant working on a 12-month contract (with possible extension) to support a single sponsor while employed by a global CRO. The role is client-facing and focuses on regulatory planning, data organization, and documentation support across global stakeholders. It emphasizes professional development and collaboration within the CRO environment and is remote-based in Mexico.
Required Skills
- Regulatory Affairs
- Project Management
- Data Analytics
- Metrics Reporting
- Database Management
- UDI Management
- Eligibility Management
- Notified Body
- Change Control
- PLM Systems
+4 more
Qualifications
- Bachelor's Degree (Life Sciences preferred)
About ClinChoice
clinchoice.comClinChoice is a full‑service global contract research organization (CRO) that helps accelerate drug and medical device approvals to market. They offer end‑to‑end clinical development, regulatory strategy, and operational support across study design, execution, data management and safety to guide sponsors through all phases of development. With global site networks, therapeutic expertise and data‑driven processes, ClinChoice aims to shorten timelines and reduce risk for development programs. They partner with biotech, pharma and device companies to navigate complex regulatory pathways and bring safer products to patients.
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