Clinical Research Coordinator

Our client, a respected clinical research organization, is seeking a detail-oriented Clinical Research Coordinator to join their Portland team. Do you thrive in a fast-paced healthcare environment? Are you passionate about advancing medical research while providing compassionate, ethical patient care? Do you have (or want to build) hands-on clinical skills like phlebotomy and EKGs? If so, this could be the perfect CRC role for you. Keep scrolling to see what this opportunity has in store. The Perks! Compensation: $20.00 - $26.00/hourly, based on experience + quarterly bonuses based on site performance 401k + 3% employer matching Health insurance, employer pays 20% of the employee’s premium Paid Time Off FSA A Day in the Life of a Clinical Research Coordinator As a CRC, you'll work closely with the site administrator, principal investigator, and sub-investigators to help bring clinical drug trials to life. You'll be the trusted point of contact for trial participants, explaining protocols, collecting samples and data, and ensuring every subject's safety and privacy are protected. Your work will directly support the integrity and success of groundbreaking clinical research. Responsibilities include: Assisting in the coordination and execution of clinical drug trials under the guidance of the site administrator, principal investigator, and sub-investigators Reading, comprehending, and executing clinical trial protocols Performing laboratory tests as required by trial protocol Monitoring clinical and laboratory data for accuracy and protocol compliance Completing all documentation required for submission to the trial sponsor Complying with all applicable international, federal, state, local, and company regulations, laws, and policies Interacting with patients, explaining trial protocols, consenting subjects, monitoring compliance, and collecting data and lab samples Protecting subject safety and maintaining patient privacy at all times Staying flexible and pitching in on other duties as needed Requirements and Qualifications: 1+ years of experience coordinating and executing clinical drug trials under the direction of site leadership and investigators Strong experience making sure trials are accurate and compliant Experience interacting with patients and explaining protocols, obtaining consent, and collecting data Skills to ensure compliance with international, federal, state, and institutional regulations and policies in your work Ability to identify and resolve data queries Strong interpersonal and communication skills High moral and ethical standards, with a professional and responsible demeanor Commitment to the success of the research team About the Hiring Company: Our client is a clinical research organization dedicated to advancing medical knowledge through well-run, participant-focused clinical trials. They value clinical excellence, integrity, and collaboration among their research staff. Come Join Our Clinical Research Team! Start by filling out this 3-minute, mobile-friendly application here. We look forward to hearing from you! #J-18808-Ljbffr IsoTalent