ApplyBlast uses AI to match you with the right jobs, tailor your resume and cover letter, and apply automatically so you can land your dream job faster.

Features

Auto Apply Resume Optimizer Cover Letter Optimizer Interview Prep

Company

Social Media

Need Help?

team@applyblast.com

Senior Associate – Regulatory Affairs (EU-OTC) at ClinChoice - ApplyBlast

Senior Associate – Regulatory Affairs (EU-OTC)

ClinChoice

4 months ago

3.3 on Glassdoor

Bengaluru, India

Onsite

Full Time

Senior

0 applicants

View Job Listing

Apply to 100+ jobs

About this role

This role involves providing managerial support for registration, renewal, and variation submissions of OTC drugs within the EMEA region. Responsibilities include compiling regulatory documentation, managing project timelines, reviewing consolidated clinical findings, and coordinating with cross-functional teams to ensure compliance and on-time delivery.

Responsibilities

Manage regulatory submission packages for drug registration and renewals
Coordinate with regional teams to ensure on-time project completion
Review consolidated clinical findings for compliance with GVP guidelines
Track license approval validity and plan renewal submissions
Update submission trackers and maintain regulatory action item tables

Skills

Qualifications

BS in ChemistryBS in Biology

About ClinChoice

clinchoice.com

Headquarters

Horsham, Pennsylvania, United States

Company Size

1001-5000 employees

Founded

1995

View Profile

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.