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 at ClinChoice - ApplyBlast

Senior Associate - Regulatory Affairs

ClinChoice

11 hours ago

3.3 on Glassdoor

Bengaluru, Karnataka, India

Onsite

Full Time

Senior

0 applicants

View Job Listing

Apply to 100+ jobs

About this role

The Senior Associate - Regulatory Affairs role involves managing regulatory events and submissions within the Veeva Vault RIM system, ensuring accurate documentation and compliance across global domains. The position requires supporting cross-functional teams with strategic and operational regulatory assistance while maintaining high data accuracy through rigorous validation and quality control processes. This role demands strong analytical skills and experience with regulatory systems to track timelines and manage health authority interactions effectively.

Responsibilities

Manage regulatory events and lifecycle submissions within Veeva Vault RIM
Perform system impact assessments and ensure accurate regulatory documentation
Track submission timelines and monitor regulatory workflows across global regions

Skills

Qualifications

B. PharmM. PharmPharm.DB.Sc (Life Sciences)M.Sc (Life Sciences)

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.