Clinical Research Coordinator (CRC)

Curaclin Research is actively hiring a Clinical Research Coordinator (CRC) for its Bhubaneswar site.

This is an excellent opportunity for B.Pharm, M.Pharm, and Life Sciences graduates looking to build or advance their careers in Clinical Research, Clinical Trial Coordination, Site Management, Regulatory Documentation, and Sponsor Communication.

🚀 WE’RE HIRING | Clinical Research Coordinator (CRC) | Curaclin Research | Bhubaneswar 🚀

Are you passionate about Clinical Research, Clinical Trials, Site Management, and Regulatory Compliance? 🧪📋✨

📢 Curaclin Research is actively hiring a Clinical Research Coordinator (CRC) for its Bhubaneswar site.

This is an excellent opportunity for B.Pharm, M.Pharm, and Life Sciences graduates looking to build or advance their careers in Clinical Research, Clinical Trial Coordination, Site Management, Regulatory Documentation, and Sponsor Communication.

If you are interested in working closely with investigators, sponsors, CROs, and clinical trial participants while gaining hands-on experience in regulated clinical studies, this opportunity could be the ideal next step in your career.

🏢 Company: Curaclin Research
🌐 Website: www.curaclinsmo.com
🏭 Industry: Clinical Research / SMO (Site Management Organization)
👉 Role: Clinical Research Coordinator (CRC)
🎓 Qualification: B.Pharm / M.Pharm / Life Sciences / Pharmacy Degree
💼 Experience: Freshers & Experienced Candidates
📍 Location: Bhubaneswar, Odisha
🏢 Work Mode: On-site
🕒 Employment Type: Full-Time

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💼 Short Job Description
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Curaclin Research is seeking dedicated and detail-oriented professionals to support clinical trial activities at its study site.

The Clinical Research Coordinator will play a critical role in ensuring smooth execution of clinical trials while maintaining compliance with ICH-GCP guidelines, study protocols, and regulatory requirements.

This role offers excellent exposure to clinical trial coordination, patient management, regulatory documentation, sponsor communication, monitoring visits, and audit readiness activities.

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🔧 Key Responsibilities
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✔ Coordinate and manage clinical trial activities at the study site
✔ Assist the Principal Investigator (PI) in conducting studies as per protocol
✔ Perform patient screening, recruitment, and follow-up coordination
✔ Maintain study documentation, Investigator Site Files (ISF), and regulatory files
✔ Ensure compliance with ICH-GCP guidelines and protocol requirements
✔ Support data entry and query resolution activities
✔ Coordinate with Sponsors, CROs, and site staff
✔ Assist during monitoring visits, audits, and regulatory inspections
✔ Ensure documentation accuracy and regulatory compliance throughout study conduct
✔ Support smooth execution of clinical trial operations and participant management

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🛠 Required Qualifications
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🎓 Educational Qualification
✅ B.Pharm
✅ M.Pharm
✅ Life Sciences
✅ Pharmacy Degree

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🎯 Required Skills & Knowledge
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✅ Knowledge of Clinical Research processes
✅ Understanding of ICH-GCP Guidelines
✅ Good Communication Skills
✅ Strong Documentation and Organizational Skills
✅ Ability to Coordinate Clinical Trial Activities
✅ Attention to Detail and Compliance-Focused Mindset
✅ Understanding of Trial Documentation and Site Operations

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⭐ Preferred Candidate Profile
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✔ Prior Site Management Experience (Preferred but Not Mandatory)
✔ Freshers with strong academic knowledge of Clinical Research can apply
✔ Understanding of GCP Guidelines and Trial Documentation Basics
✔ Ability to work effectively with investigators, sponsors, CROs, and site teams
✔ Strong interpersonal and coordination skills
✔ Passion for building a career in Clinical Research

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✨ Why Join Curaclin Research?
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✨ Hands-on exposure to real-time Clinical Trial Management
✨ Experience in Regulatory Documentation and Audit Readiness
✨ Direct interaction with Sponsors and CROs
✨ Strong foundation for future roles such as Clinical Research Associate (CRA) or Site Manager
✨ Career growth opportunities in the expanding Clinical Research industry
✨ Exposure to site management and regulatory compliance processes
✨ Opportunity to work in a regulated and quality-driven clinical environment

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🏢 About Curaclin Research
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Curaclin Research is a Clinical Research and Site Management Organization (SMO) focused on supporting high-quality clinical trial execution while maintaining regulatory compliance and participant safety.

The organization collaborates with sponsors, CROs, investigators, and healthcare professionals to facilitate successful clinical studies and contribute to medical innovation.

🚀 Core Focus Areas:
✅ Clinical Trial Management
✅ Site Management Services
✅ Regulatory Documentation
✅ Patient Recruitment & Retention
✅ Clinical Operations Support
✅ Audit & Inspection Readiness
✅ Sponsor & CRO Coordination

Curaclin Research provides an excellent platform for aspiring clinical research professionals to gain practical industry experience and build long-term careers in clinical operations.

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🚀 Career Growth Opportunities
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This role serves as an excellent stepping stone toward careers such as:

✅ Clinical Research Associate (CRA)
✅ Senior Clinical Research Coordinator
✅ Clinical Trial Coordinator
✅ Site Manager
✅ Clinical Operations Specialist
✅ Regulatory Affairs Professional

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📩 Apply Now
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Interested candidates can send their updated resume to:
📧 hr.curaclinresearch@gmail.com
📧 bd@curaclinsmo.com

🌐 Website: www.curaclinsmo.com

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⚡ If you’re looking to build a successful career in Clinical Research, Clinical Trial Coordination, Site Management, and Regulatory Compliance, Curaclin Research offers an excellent opportunity to gain hands-on industry exposure and accelerate your professional growth.