Senior Associate - Regulatory Affairs (Reg Ops EU MDR)

ClinChoice

1 month ago

3.3 on Glassdoor

Remote

Full Time

Senior

0 applicants

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About this role

A Senior Associate in Regulatory Affairs (Reg Ops EU MDR) at ClinChoice supports the company’s regulatory operations for medical devices, with emphasis on EU Medical Device Regulation (EU MDR) compliance and submission maintenance. The role is part of ClinChoice’s global regulatory affairs function serving pharmaceutical and medical device clients. The position is based in Bengaluru, offered as a full-time remote role, and targets candidates with 4–6 years of experience.

Skills

Qualifications

Bachelor's Degree (Life Sciences Preferred)

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.