Looking for work-from-home pharma jobs? Monroe Biomedical Research is hiring a Regulatory Support Specialist for remote work in India. This is a great opportunity for clinical research professionals to build a career in regulatory affairs while working with global teams.
About the Company
Monroe Biomedical Research is a growing Clinical Research Organization (CRO) focused on regulatory excellence, patient safety, and high-quality clinical studies. The company supports innovative treatments through strong compliance and operational efficiency.
Job Overview
- Company: Monroe Biomedical Research
- Role: Regulatory Support Specialist
- Location: Remote (India)
- Experience: 1+ Years
- Qualification: Bachelor’s Degree or Equivalent
- Job Type: Full-time Remote
Skills Required
- Experience in clinical research or regulatory support
- Strong organizational and documentation skills
- Excellent English communication
- Proficiency in Microsoft Office
- Ability to manage multiple tasks efficiently
- Knowledge of FDA regulations & ICH-GCP (preferred)
Key Responsibilities
- Assist with IRB submissions and amendments
- Maintain electronic regulatory documentation
- Track submission timelines and approvals
- Collect and manage essential documents (CVs, licenses)
- Ensure compliance with regulatory standards
- Support audit and inspection readiness
- Collaborate with global clinical teams
Benefits & Perks
- 100% remote work flexibility
- Career growth in regulatory affairs
- Exposure to global clinical research operations
- Competitive salary package
- Opportunity to contribute to healthcare innovation
How to Apply
👉 Apply online through the official careers portal:
🌐 Monroe Biomedical Research Careers
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Monroe Biomedical Research career page.
Why You Should Apply
This role is ideal for professionals who want to transition into regulatory affairs and global clinical research while enjoying the flexibility of remote work. You will gain valuable experience in IRB processes, compliance, and international study operations.
FAQs
1. Is this a remote job?
Yes, this is a full-time remote position for candidates in India.
2. What experience is required?
Minimum 1 year in clinical research or regulatory support.
3. What qualification is needed?
Bachelor’s degree or equivalent.
4. Is GCP knowledge required?
Preferred but not mandatory.
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