Regulatory Affairs Specialist – Consultant

ClinChoice(1 month ago)

RemoteContractSenior$131,165 - $178,765 (estimated)Regulatory Affairs

About this role

A Regulatory Affairs Specialist – Consultant (Sr. Product License Maintenance Manager, PLM Compliance Support) is a client-facing regulatory professional employed by a global CRO to support a single sponsor on a 12-month contract. Based remotely in Mexico, the role focuses on maintaining regulatory compliance and product license portfolios while collaborating with internal and external stakeholders. The position requires strong regulatory knowledge, attention to quality, and the ability to operate within tight timelines.

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Required Skills

Certificate Review
NDA Reports
Drug Listings
Annual Reports
Filing Deadlines
Stakeholder Liaison
Legalization Management
Communication
Project Management
Escalation Management

+8 more

Qualifications

Bachelor’s Degree

About ClinChoice

clinchoice.com

ClinChoice 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.