The world of clinical research is evolving rapidly, and decentralized trials are opening doors for remote career opportunities like never before. Koncord Clinical Research Services is currently hiring Pharm D Graduates for the role of Regulatory Coordinator — and yes, it’s 100% Work From Home.
If you’ve recently completed your Doctor of Pharmacy (Pharm D) and are looking for a corporate role that blends clinical expertise with regulatory precision, this could be your ideal first step. 🏠💻
What is a Regulatory Coordinator? 🧐
In clinical research, every study must comply with strict legal and ethical guidelines. Regulatory authorities such as the:
- U.S. Food and Drug Administration (FDA)
- European Medicines Agency (EMA)
set standards that sponsors and research sites must follow.
A Regulatory Coordinator ensures that:
- Ethics approvals are secured
- Trial documentation is complete and audit-ready
- Regulatory submissions are filed on time
- Compliance with Good Clinical Practice (GCP) is maintained
It’s a role defined by accuracy, ethics, and organization.
Job Details: Koncord Clinical Research Services 🏥
- Job Role: Regulatory Coordinator
- Qualification: Pharm D Graduate 🎓
- Experience: Freshers Welcome 🆕
- Work Type: 100% Remote / Work From Home 🌐
- Organization: Koncord Clinical Research Services
Why This Role is Perfect for Pharm D Graduates 💊
Many Pharm D graduates consider hospital pharmacy or clinical practice. However, Regulatory Affairs (RA) offers a high-growth corporate pathway.
✔ Remote Flexibility
Work from anywhere without relocation stress.
✔ Fresher-Friendly Entry
Specialized regulatory roles typically demand 2–3 years’ experience. This opening allows you to start fresh.
✔ Core Science Application
You’ll review clinical protocols, safety documents, and investigator brochures — where your pharmacology knowledge becomes a major advantage.
Key Responsibilities 📝
As a Regulatory Coordinator, your daily tasks may include:
- 📂 Documentation Management – Maintaining Trial Master Files (TMF) & Investigator Site Files (ISF)
- ⚖️ Compliance Monitoring – Ensuring adherence to GCP and regulatory guidelines
- 🏛️ Ethics Committee Liaison – Coordinating with Institutional Review Boards (IRBs) or Ethics Committees
- ⏳ Submission Tracking – Monitoring deadlines for amendments, safety reports & renewals
- 📧 Professional Communication – Acting as a bridge between sponsors, sites & authorities
Essential Skills for Success 💡
Since this is a remote role, strong self-management is crucial:
- Self-Discipline & Time Management ⏰
- Attention to Detail (Regulatory work demands precision)
- Digital Literacy (Cloud storage, document systems, Zoom/Teams)
- Professional Written Communication
Career Path: Where Can This Lead? 📈
Starting as a Regulatory Coordinator opens multiple high-growth pathways:
- Regulatory Affairs Associate / Manager
- Quality Assurance (QA) Auditor
- Clinical Project Manager
- Pharmacovigilance Specialist
With experience, professionals in Regulatory Affairs often move into global regulatory roles, working directly with authorities across the US, EU, and other markets.
How to Apply 📩
If you meet the eligibility criteria, apply promptly.
Application Instructions:
- Update your CV highlighting:
- Pharm D projects
- Internships
- GCP knowledge
- Any regulatory exposure
- 📧 Send your CV to: hr@koncordclinical.com
- Suggested Subject Line:
Application for Regulatory Coordinator – Pharm D Graduate – [Your Name]
Final Thoughts 🌟
For a Pharm D fresher, transitioning into the corporate clinical research world can feel overwhelming. However, joining Koncord Clinical Research Services as a Remote Regulatory Coordinator offers:
- Structured learning
- Exposure to global regulatory standards
- Long-term career stability
- Work-from-home flexibility
This is more than just a job — it’s a strategic entry into the regulatory ecosystem of drug development. 🚀
Prepare your resume carefully, review formatting twice, and take that confident first step toward a rewarding career in Clinical Research.
