Clinical Research Coordinator

17 hours ago

Ahmedabad, Gujarat, India 47b723d7-39fb-49e9-8e6b-e5a8eba7edb4 Full time ₹ 5,00,000 - ₹ 15,00,000 per year

Company Description

Sapientia Medicus Research is a global leader in Site Management Organization (SMO) services with presence in India and Canada, specializing in supporting clinical research in various therapeutic areas such as oncology, ophthalmology, nephrology, and more. Known for its expertise in rapid patient enrollment and accurate data collection, the company ensures the success of both local and international clinical trials. With a commitment to Good Clinical Practice (GCP) standards, the organization delivers high-quality research without compromising data integrity. Sapientia Medicus Research is passionate about advancing healthcare through collaborative global research efforts and contributing to the discovery of innovative treatments.

Role Description

This is a full-time, on-site role for a Clinical Research Coordinator located in Barrie, ON. Responsibilities include coordinating and managing clinical trials, ensuring informed consent is obtained, compliance with protocols, and maintaining accurate and complete research records. The Clinical Research Coordinator will work closely with investigators, sponsor representatives, and other team members to ensure studies are executed in adherence to Good Clinical Practice (GCP) and regulatory requirements.

Qualifications

  • Expertise in Informed Consent procedures and Protocol adherence.
  • Strong background in Clinical Research Experience and participation in Clinical Trials.
  • Proficiency in conducting and supporting Research activities with a comprehensive understanding of GCP guidelines.
  • Excellent organizational, communication, and problem-solving skills.
  • Ability to work independently while collaborating effectively with diverse teams.
  • Previous experience in coordinating or managing clinical trials is highly desirable.
  • Relevant educational background such as a degree in life sciences, nursing, or related fields is preferred.
  • Familiarity with ethical standards and local regulatory requirements for clinical trials is an asset.

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