Clinical Research Coordinator

Company Description

Concept Clinical Service is a Research Management Organization dedicated to supporting the execution and success of clinical trials across the pharmaceutical, biotechnology, and medical device industries. With expertise in adhering to protocols, maintaining quality data, and ensuring compliance with ICH-GCP and regulatory standards, we focus on delivering ethically sound and highly specialized services to meet diverse client needs. Our offerings include study design, regulatory consulting, patient recruitment, medical writing, and clinical monitoring. Recognized for our expertise in rare diseases, particularly in India, we are committed to delivering exceptional service and fostering strong partnerships within the research community. Our experienced team strives to make a meaningful impact through innovative and customized solutions.

Role Description

This is a full-time on-site role based in Surat for a Clinical Research Coordinator. In this role, you will manage and oversee day-to-day clinical trial activities, ensuring adherence to protocols and regulatory requirements. Responsibilities include coordinating informed consent processes, maintaining study documentation, monitoring clinical trial progress, and ensuring high-quality data collection and reporting. You will collaborate with research teams and investigators, support patient recruitment efforts, and facilitate communication with study sponsors and other stakeholders.

Qualifications

• Proficiency in obtaining Informed Consent and knowledge of Protocol development and adherence.
• Strong background in Research, Clinical Research Experience, and understanding of Clinical Trials.
• Exceptional organizational, documentation, and communication skills.
• Ability to work collaboratively with multidisciplinary teams and adapt to dynamic environments.
• Knowledge of ICH-GCP guidelines and regulatory compliance is preferred.
• Bachelor's degree in Life Sciences, Nursing, or related field is required; advanced degrees are a plus.
• Experience in rare disease research and patient recruitment is advantageous.