Clinical Research Coordinator

Company Description

Triethix Clinical Research is a clinician-led Site Management Organization (SMO) based in Ahmedabad, India, specializing in efficient and compliant execution of clinical trials. Focused on optimizing trial site operations, Triethix collaborates with CROs, sponsors, and investigators to deliver expertise in site feasibility, startup strategy, regulatory coordination, patient recruitment, and protocol adherence. With leadership from a pulmonologist and medical director, the organization ensures real-world clinical relevance in its research studies. Triethix is committed to advancing clinical research partnerships and multi-site trials with a patient-centric approach.

Role Description

This is a full-time, on-site Clinical Research Coordinator position based in Junagadh City. In this role, the coordinator will oversee the day-to-day operations of clinical trials, including patient screening, informed consent procedures, and adherence to study protocols. They will also manage regulatory documentation, ensure safety monitoring, and maintain protocol compliance. The role involves collaboration with investigators and study teams to ensure the successful execution of clinical research projects.

Qualifications

• Strong knowledge and experience with Informed Consent procedures and compliance
• Proficiency in understanding and managing study Protocol requirements
• Background in Research and prior Clinical Research Experience
• Familiarity with Clinical Trials operations and processes
• Excellent organizational, communication, and time-management skills
• Ability to work collaboratively in a team-oriented environment
• Bachelor's degree in a relevant field such as healthcare, life sciences, or related disciplines
• Experience in handling regulatory documents and ethical committee coordination is an advantage