Clinical Research Coordinator (CRC)

Why This Role Matters

The Clinical Research Coordinator (CRC) plays a crucial role in ensuring the smooth execution of clinical trials at the site level. Clinical research is highly regulated and process-driven, where accuracy, compliance, and patient safety are critical. The CRC acts as the operational backbone of the study, ensuring that protocols are followed precisely and regulatory standards are maintained.
This position directly contributes to advancing medical research by supporting the Principal Investigator (PI), coordinating patient activities, and maintaining high-quality documentation. For professionals with a pharmacy or life sciences background, this role offers strong career progression into clinical operations, site management, and regulatory affairs.

Job Description

Curaclin Research is hiring a Clinical Research Coordinator (CRC) in Bhubaneswar, Odisha. This opportunity is ideal for candidates with 1–2 years of clinical research experience who are looking to strengthen their expertise in site management and clinical trial operations.
The CRC will coordinate daily clinical trial activities, assist investigators, ensure regulatory compliance, and maintain study documentation in accordance with ICH-GCP guidelines. The role requires strong organizational skills, attention to detail, and the ability to collaborate effectively with sponsors, CROs, and site teams.

Key Features of the Role

• Site coordination Direct involvement in managing clinical trial activities at the research site
• Regulatory exposure Hands-on experience with essential documents and compliance standards
• Patient interaction Participation in screening, recruitment, and follow-up processes
• Sponsor collaboration Regular communication with Sponsors and CROs
• Audit readiness Exposure to monitoring visits and regulatory inspections
• Career growth Strong foundation for advancement in clinical operations

Responsibilities

• Trial management Coordinate and manage clinical trial activities at the site
• PI support Assist the Principal Investigator in conducting studies as per approved protocol
• Patient coordination Perform patient screening, recruitment, enrollment, and follow-up scheduling
• Documentation Maintain regulatory binders, essential documents, and study files
• Compliance Ensure adherence to ICH-GCP guidelines and protocol requirements
• Data handling Perform accurate data entry and support query resolution
• Stakeholder coordination Communicate effectively with Sponsors, CROs, and internal staff
• Monitoring support Assist during monitoring visits, audits, and inspections

Required Qualifications

• Educational background B.Pharm, M.Pharm, Life Sciences, or Pharmacy degree
• Experience 1–2 years of clinical research experience (site experience preferred)
• GCP knowledge Understanding of ICH-GCP guidelines and clinical research processes
• Communication Strong verbal and written documentation skills
• Regulatory awareness Knowledge of essential documents and regulatory file maintenance
• Organizational skills Ability to manage multiple tasks with accuracy

Educational Requirements

• Bachelor’s or Master’s degree in Pharmacy or Life Sciences

Experience and Skills

• Clinical exposure Experience in patient recruitment and study coordination
• Regulatory documentation Familiarity with investigator site file maintenance
• Data accuracy Strong attention to detail in data entry and reporting
• Team collaboration Ability to work closely with investigators and cross-functional teams
• Time management Capability to meet study timelines and compliance requirements

Salary Insights

Estimated Salary Range: ₹2,40,000 – ₹3,60,000 per annum (CTC)
The salary range is based on industry standards for Clinical Research Coordinators with 1–2 years of experience in India. Compensation may vary depending on site experience, skill set, and interview performance.

Company Overview

Curaclin Research is a clinical research organization focused on supporting clinical trial execution and site management activities. The organization works closely with investigators, sponsors, and research teams to ensure studies are conducted in compliance with regulatory standards and ethical guidelines.
Curaclin Research emphasizes quality-driven processes, regulatory adherence, and professional development within clinical operations.

FAQs

• Is prior hospital experience mandatory?
Not mandatory, but site-based clinical research experience is preferred

• Is travel required?
Primarily site-based role; travel may depend on study requirements

• Does the role involve patient interaction?
Yes, patient screening and follow-up coordination are key responsibilities
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• What growth opportunities are available?
Career progression into Senior CRC, Clinical Research Associate (CRA), or Clinical Operations roles

Application Tips

• Highlight site experience Clearly mention involvement in clinical trial coordination
• Emphasize GCP knowledge Include certifications or training in ICH-GCP
• Showcase documentation skills Provide examples of regulatory file handling
• Demonstrate patient coordination Experience in recruitment and follow-up management
• Keep resume structured Ensure accuracy and professional formatting
• Mention software familiarity If experienced with EDC systems or CTMS, include details