Sr. Regulatory Affairs Associate- CONSULTANT
ClinChoice(28 days ago)
About this role
A Senior Regulatory Affairs Associate Consultant hired through a global CRO to support a single sponsor on a 12-month contract (possible extension). The role is client-facing and sits within the CRO’s regulatory team, providing regulatory subject-matter support and acting as a liaison between the sponsor and CRO. The position is remote and based in Mexico.
Required Skills
- Regulatory Affairs
- EU MDR
- FDA Regulations
- ISO 13485
- Document Review
- Document Management
- Quality Control
- PLM Systems
- Adobe Acrobat
- Stakeholder Management
+2 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.
Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at ClinChoice
Similar Jobs
Senior Regulatory Affairs Specialist
Hyperfine(1 month ago)
Regulatory Affairs Manager (Atlanta)
CorDx(8 months ago)
Lead Regulatory Affairs Specialist
Dozee(15 days ago)
Head of Quality & Regulatory Affairs
Until(1 month ago)
Regulatory & Compliance Specialist
CorDx(1 year ago)
Senior Regulatory Affairs Specialist
Hyperfine(1 month ago)