Join our innovative research team as a Clinical Research Coordinator, where you will be instrumental in advancing medical science and patient care. We are seeking a highly organized and detail-oriented individual to manage and coordinate clinical trials from inception to completion. This role involves ensuring strict adherence to study protocols, regulatory requirements (ICH-GCP, FDA), and ethical guidelines. You will serve as a primary liaison between investigators, patients, and sponsors, facilitating smooth trial operations and contributing directly to the development of new therapies and interventions. If you are passionate about healthcare innovation and thrive in a dynamic research environment, we encourage you to apply. Skills: ICH-GCP Guidelines, FDA Regulations, Clinical Trial Management, Electronic Data Capture (EDC) Systems, Electronic Medical Records (EMR), Patient Recruitment and Retention, Source Document Review, Regulatory Document Preparation, Budget Management, Strong Organizational Skills, Excellent Written and Verbal Communication, Problem-Solving, Attention to Detail, Medical Terminology, Time Management Requirements: Bachelor's degree in a scientific, healthcare, or related field (e.g., Nursing, Biology, Public Health), Minimum of 2-3 years of experience in clinical research coordination or a related role, Demonstrated understanding of the clinical research process and regulatory landscape, Proficiency in Microsoft Office Suite (Word, Excel, Outlook, PowerPoint), Ability to work independently and collaboratively within a team environment, Strong interpersonal skills with a compassionate and professional demeanor, Certification as a Clinical Research Coordinator (CCRC or CCRP) is preferred but not required, Ability to manage multiple priorities and meet deadlines in a fast-paced setting, Commitment to ethical conduct and patient safety Join our innovative research team as a Clinical Research Coordinator, where you will be instrumental in advancing medical science and patient care. We are seeking a highly organized and detail-oriented individual to manage and coordinate clinical trials from inception to completion. This role involves ensuring strict adherence to study protocols, regulatory requirements (ICH-GCP, FDA), and ethical guidelines. You will serve as a primary liaison between investigators, patients, and sponsors, facilitating smooth trial operations and contributing directly to the development of new therapies and interventions. If you are passionate about healthcare innovation and thrive in a dynamic research environment, we encourage you to apply.

Skills:
ICH-GCP Guidelines, FDA Regulations, Clinical Trial Management, Electronic Data Capture (EDC) Systems, Electronic Medical Records (EMR), Patient Recruitment and Retention, Source Document Review, Regulatory Document Preparation, Budget Management, Strong Organizational Skills, Excellent Written and Verbal Communication, Problem-Solving, Attention to Detail, Medical Terminology, Time Management

Requirements:
Bachelor's degree in a scientific, healthcare, or related field (e.g., Nursing, Biology, Public Health), Minimum of 2-3 years of experience in clinical research coordination or a related role, Demonstrated understanding of the clinical research process and regulatory landscape, Proficiency in Microsoft Office Suite (Word, Excel, Outlook, PowerPoint), Ability to work independently and collaboratively within a team environment, Strong interpersonal skills with a compassionate and professional demeanor, Certification as a Clinical Research Coordinator (CCRC or CCRP) is preferred but not required, Ability to manage multiple priorities and meet deadlines in a fast-paced setting, Commitment to ethical conduct and patient safety