Looking to start or grow your career in Regulatory Affairs? 🌍📑
Here’s a solid opportunity for freshers and early-career professionals who want hands-on exposure to global regulatory systems. ClinChoice is hiring for Associate – Regulatory Affairs (RegPoint) at its Bengaluru office.
If you come from a Pharmacy or Life Sciences background and are curious about regulatory systems, compliance, and structured data management, this role can be a strong launchpad for a long-term career in pharma and clinical research 🚀.
🏢 About ClinChoice
ClinChoice is a globally recognized organization delivering end-to-end solutions across clinical research, regulatory affairs, pharmacovigilance, biometrics, and medical affairs. Founded in 1995, the company partners with leading pharmaceutical, medical device, and consumer healthcare organizations worldwide.
With operations across India, the US, UK, China, Japan, the Philippines, Armenia, and Mexico, ClinChoice supports both local and global regulatory compliance 🌐. Known for its technology-driven approach and deep domain expertise, the company offers structured processes and real-world regulatory exposure—ideal for professionals building a regulatory career.
📌 Job Details at a Glance
- Job Title: Associate – Regulatory Affairs (RegPoint)
- Employment Type: Full-time, Permanent
- Location: Bengaluru, India
- Work Mode: Office-based
- Experience: Fresher to 1 year (0–6 months preferred)
- Education: B.Pharm / M.Pharm
👉 This role is well-suited for fresh graduates and candidates with limited exposure to RIMS / regulatory data management.
🔍 Key Responsibilities – What Will You Do?
✅ Primary Responsibilities
Your core focus will be Regulatory Information Management Systems (RIMS) and ensuring data accuracy:
- Perform regulatory data clean-up as per defined processes
- Review and verify data entered into the RIMS platform
- Update and validate records to support business users
- Handle daily user requests and regulatory tickets
- Communicate clearly with internal stakeholders on data queries
- Process submission intake requests efficiently
🧠 You’ll gain a clear understanding of how regulatory data flows across global systems and submissions.
📂 Secondary Responsibilities
Beyond core tasks, you’ll also support data collection and quality control:
- Collect regulatory information from manual and electronic sources
- Enter and track regulatory data in RIMS
- Perform peer quality checks against source documents
- Ensure strict compliance with SOPs and quality standards
These responsibilities sharpen your attention to detail and compliance mindset 🔍✔️.
👩🎓 Candidate Profile – Who Can Apply?
🎓 Educational Qualification
- B.Pharm or M.Pharm (mandatory)
💼 Experience
- Freshers are welcome
- 3–6 months of experience in RIMS or regulatory data management is a plus
💻 Skills Required
- Basic to intermediate MS Office skills
- Familiarity with RIMS / document management systems (preferred, not mandatory)
- Strong English communication skills (written & verbal)
- Comfortable working in a process-driven, office-based environment
🌱 Why This Role Is Great for Freshers
If you’re just starting out, this role checks many boxes:
✨ Exposure to global regulatory operations
✨ Hands-on experience with RIMS platforms
✨ Strong learning curve in compliance & documentation
✨ Interaction with international teams and processes
✨ A reliable entry point into Regulatory Affairs, RIMS, or Clinical Operations
Many professionals use roles like this to progress into Regulatory Specialists, Submission Managers, or Global Regulatory Leads 📈.
🔗 Apply Now
👉 LinkedIn Job Link: https://www.linkedin.com/jobs/view/4369104731
🏁 Final Thoughts
The Associate – Regulatory Affairs (RegPoint) role at ClinChoice is a promising opportunity for freshers and early-career professionals aiming to build a future in regulatory affairs. With structured workflows, global exposure, and hands-on system experience, this position offers a practical and stable start in the industry.
If you’re detail-oriented, eager to learn, and interested in regulatory systems, this could be a smart next move for your career 💼✨.
