About the Company
ClinChoice is a leading full-service global Clinical Research Organization (CRO) with over three decades of experience. The company specializes in accelerating drug and medical device development through innovative, high-quality solutions.
ClinChoice supports biopharmaceutical, vaccine, and consumer health clients worldwide. It maintains an outstanding reputation for regulatory expertise, clinical operations, and data management.
Job Details
- Company Name: ClinChoice
- Experience: 0–3 years
- Location: Bengaluru, India
- Work Type: Full-time, On-site
Job Description
ClinChoice seeks a motivated Associate – Regulatory Affairs (RMQ), also known as RM Data Associate, for its Bengaluru office. This entry-level role focuses on raw material data management in regulatory affairs.
It offers excellent exposure to global stakeholders, supplier communications, and technical regulatory requirements across cosmetics, OTC, drugs, and nutritionals.
Associate – Regulatory Affairs (RMQ)
- Designation: Associate / RM Data Associate
- Experience: 0–3 years
- Key Focus: End-to-end raw material data request governance and technical regulatory support
Skills and Qualifications
- Strong understanding of regulatory requirements for raw materials (cosmetics, OTC, drugs, food/nutritionals)
- Knowledge of toxicology and safety assessment data
- Excellent project and time management for high-volume requests
- Superior attention to detail and disciplined process execution
- Effective communication (internal, external suppliers, global stakeholders)
- Problem-solving and critical thinking abilities
- Sense of urgency, learning agility, and resilience in fast-paced environment
Key Responsibilities
- Initiate requests within 24 hours and adhere to TAT
- Seek clarifications and handle supplier communications
- Escalate delays timely and update Global Request Tracker (GTR)
- Ensure transparent stakeholder communication
- Maintain high technical accuracy in data collection/entry
- Collaborate with toxicology partners for specific needs
- Achieve KPIs for quality, productivity, and right-first-time delivery
- Demonstrate ownership for complete, on-time request resolution
Benefits and Perks
- Competitive entry-level salary
- Comprehensive training and mentorship
- Global exposure in a leading CRO
- Career progression in regulatory affairs
- Collaborative and innovative work culture
- Opportunity to contribute to drug development
How to Apply
Apply directly through the ClinChoice careers portal or official job listing. Visit ClinChoice Careers to explore openings and submit your application. For this specific role, check platforms like LinkedIn or the company’s Greenhouse portal for the latest posting.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the ClinChoice Career page.
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Why You Should Join ClinChoice
ClinChoice provides a supportive environment for early-career professionals to grow in regulatory affairs and clinical research. With a global footprint and focus on innovation, employees gain valuable experience in high-impact projects.
The company fosters learning agility, ownership, and collaboration, making it an ideal launchpad for long-term success in the pharmaceutical and CRO industry.