AlphaWorks Pvt Ltd

Join our innovative healthcare team dedicated to advancing medical knowledge and patient care through cutting-edge research. We are seeking a meticulous and highly organized Clinical Research Coordinator to manage and execute clinical trials across various therapeutic areas. In this role, you will be responsible for the day-to-day operations of clinical studies, ensuring compliance with all regulatory requirements, ethical standards, and study protocols. You will play a crucial role in patient recruitment, data collection, and maintaining accurate study documentation, contributing directly to the success of groundbreaking medical discoveries.

Skills:
Clinical trial management, ICH-GCP guidelines, FDA regulations, Patient recruitment and retention, Informed consent process, Data collection and entry, Electronic Data Capture (EDC) systems, Electronic Medical Records (EMR), Medical terminology, Strong organizational skills, Excellent written and verbal communication, Attention to detail, Problem-solving, Microsoft Office Suite

Requirements:
Bachelor's degree in a scientific, healthcare, or related field., Minimum of 2-3 years of experience coordinating clinical trials, preferably in an academic or hospital setting., Demonstrated understanding and application of ICH-GCP guidelines and FDA regulations., Proficiency with clinical trial management software and EDC systems., Ability to work independently and manage multiple research protocols simultaneously., Strong interpersonal skills with the ability to interact professionally with patients, sponsors, and colleagues., Certification as a Clinical Research Coordinator (CCRC or CCRP) is highly preferred.