Senior Research Coordinator

Manage 2–6 trials of varying complexity, perform clinical procedures, and lead study coordination from start to finish. Work closely with investigators, sponsors, and monitors while mentoring junior staff and contributing to internal training. Be part of a supportive team that values initiative, adaptability, and continuous learning. Experience the synergy of working within a local SMO backed by the resources and reach of a global CRO. Requirements Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens. Solid understanding of site operations and the drug development process. CRC I: Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants. CRC II: Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants. Strong written and verbal communication skills, with attention to detail and time management. Comfortable using CTMS, eCRFs, and Microsoft Office tools. Demonstrates expertise in managing clinical trials, including obtaining vital signs, performing phlebotomy, and conducting ECGs. Proficient in site operations and the drug development process, with strong communication and time management skills. Highest-signal resume keywords Clinical Research Coordination Phlebotomy ECG Conducting CTMS Usage ECRF Management ATS Optimization Keywords Hard Skills Vital Signs Acquisition Lab Specimen Processing Clinical Trial Management Drug Development Process Clinical Research Experience Soft Skills Written Communication Verbal Communication Attention to Detail Time Management Adaptability Industry Keywords Clinical Research Investigative Site Study Coordination Trial Management Continuous Learning Tools & Technologies CTMS ECRFs Microsoft Office #J-18808-Ljbffr