Applying for Associate - Regulatory Affairs at ClinChoice? Compare this live job with your resume first.

🎯 Tailor my resume
←Jobiba.Me
C
Active22h ago

Associate - Regulatory Affairs

ClinChoice·📍 Chennai, Tamil Nadu, India

Employment

CONTRACT

Work mode

On-site

Experience

0 months–2 years

Salary

Not disclosed

Salary not disclosed

Check market pay for comparable Associate roles before applying.

Salary →

Role overview

Job description

Job Title: Associate – Regulatory Affairs Employment Type: Contract, Full-time Location: Chennai, India Work Type: Office-based Experience: 0–2 years About ClinChoice ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology to help our partners advance healthcare by accelerating clinical trials with data-driven insights, delivering the best strategies for product registration, and enhancing patient safety through real-world and clinical analyses. Our global delivery network has expanded to centers and satellite offices in the United States, Mexico, the United Kingdom, Armenia, China, Japan, India, and the Philippines to help our customers maintain regulatory compliance locally

…

About this listing

  • Source: ClinChoice's official careers site (via Greenhouse) · last confirmed on the source 3 Nov 2026
  • Posted 2 Nov 2026

Jobiba does not charge job seekers. Never pay to apply or share OTPs, card or bank details.

Role market pulse

How ASSOCIATE demand looks in India

80/100 · hot

Live jobs

5,224

Posted 30d

2,973

30d movement

+304.5%

Remote share

0%

Salary listed

0.3%

Salary trend 1Y

Not enough history

What they are looking for

Skills & requirements

Qualification

Experience with xEVMPD (Extended Eudravigilance Medicinal Product Dictionary). • Knowledge of pharmaceutical regulatory affairs and lifecycle management. • Experience with regulatory submission tools and databases. Why Join Us? • Work on high-impact regulatory projects in a global environment. • Opportunity to develop expertise in IDMP compliance and data management. • Collaborate with industry experts and enhance your regulatory knowledge. If you are passionate about regulatory data management and ensuring compliance with evolving global standards, we encourage you to apply!

Department · Regulatory Affairs

Hiring company

ClinChoice

Healthcare

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 30 years of proven high-quality delivery and results across all our services with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. We are on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Join our passionate team and make a meaningful impact on global healthcare!

Related opportunities

Similar active roles

Relevant, currently active roles for this market.

All jobs →

🔔 Get job alerts

New Associate jobs in Chennai, Tamil Nadu, India, straight to your inbox.

No spam · Unsubscribe anytime