Clinical Research Coordinator

Summary The role of Senior Clinical Research Coordinator involves managing multiple clinical trials across various therapeutic areas, ensuring regulatory compliance, and conducting clinical procedures. Responsibilities include recruiting participants, obtaining informed consent, coordinating study activities from start to finish, and collaborating with investigators, sponsors, and monitors. The position also requires mentoring junior staff and contributing to training programs. Qualifications include 1-3 years of clinical research experience at an investigative site, proficiency in vital signs, phlebotomy, ECGs, and lab processing. Candidates should have a solid understanding of site operations and drug development, excellent communication skills, and experience with CTMS, eCRF systems, and Microsoft Office. The role demands strong attention to detail and the ability to support various trial activities efficiently.