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Clinical Research Coordinator Job Metta Clinical

Job Opportunity: Clinical Research Coordinator (CRC) at Metta Clinical

Job Summary
Metta Clinical is seeking a detail-oriented and motivated Clinical Research Coordinator (CRC) to join our team in Raipur, Chhattisgarh. This is an excellent opportunity for pharmacy or life science graduates with clinical trial experience to play a pivotal role in supporting investigators, managing trial operations, and contributing to advancements in healthcare. We are looking for a dedicated professional who is committed to maintaining high standards of data integrity and regulatory compliance.


Job Overview

  • Role: Clinical Research Coordinator (CRC)
  • Company: Metta Clinical
  • Location: Raipur, Chhattisgarh, India (On-site)
  • Industry: Clinical Research / Healthcare
  • Experience Required: 1–2 Years in Clinical Trials
  • Qualification: B.Pharm or Science Graduate (Life Sciences preferred)
  • Application Deadline: 1 April 2026
  • Compensation: ₹2.4 LPA – ₹4.0 LPA (commensurate with experience)

Key Responsibilities

As a Clinical Research Coordinator, you will serve as a vital link between clinical investigators, study participants, and regulatory bodies. Your primary responsibilities will include:

  • Protocol Management: Overseeing the coordination of clinical trials in strict accordance with approved protocols and regulatory guidelines.
  • Study Lifecycle Support: Assisting Principal Investigators with all phases of the study, including site initiation, day-to-day execution, and final study closure.
  • Documentation Excellence: Maintaining accurate and timely clinical trial documentation, including Informed Consent Forms (ICF), Case Report Forms (CRF), and comprehensive source data.
  • Participant Management: Managing patient recruitment efforts, ensuring proper informed consent, and conducting regular participant follow-ups to maintain study retention.
  • Compliance & Quality Assurance: Ensuring total adherence to Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and relevant regulatory requirements.
  • Operational Readiness: Preparing the site for monitoring visits and audits to ensure all records meet high-quality standards.
  • Data Reporting: Facilitating precise data collection, entry, and reporting to ensure the reliability of trial results.

Qualifications & Skills

To be successful in this role, you should possess the following qualifications and professional competencies:

  • Educational Background: A Bachelor’s degree in Pharmacy (B.Pharm) or a related Science field (Life Sciences preferred).
  • Experience: A minimum of 1–2 years of hands-on experience working within a clinical trial environment.
  • Technical Knowledge: A solid understanding of ICH-GCP guidelines, the clinical trial lifecycle, and complex regulatory documentation.
  • Professional Skills: Excellent interpersonal, communication, and organizational skills. You must be able to coordinate effectively with diverse teams and manage multiple tasks simultaneously.
  • Location: Preference will be given to local candidates residing in or near Raipur.

Benefits

Joining Metta Clinical offers more than just a job; it provides a platform for long-term professional development. Benefits of this position include:

  • Competitive Compensation: A salary package tailored to your experience and skills.
  • Direct Exposure: Hands-on, real-time experience in clinical research operations, giving you a comprehensive understanding of the trial ecosystem.
  • Career Advancement: This role serves as a strong foundation for future career growth into specialized domains such as Clinical Research Associate (CRA), Clinical Data Management (CDM), or Pharmacovigilance (PV).
  • Professional Impact: The opportunity to contribute to life-saving research and healthcare innovation.

How to Apply

We invite qualified candidates who are passionate about clinical research to apply for this position. Please ensure your application is submitted on or before the deadline of 1 April 2026.

Please prepare your updated resume highlighting your clinical trial experience and current certifications, and submit it through our official application portal or the designated contact channel provided by the hiring team.

We look forward to reviewing your application and exploring how you can contribute to the mission of Metta Clinical.