Clinical Research Coordinator I

Job summary
Assists investigators as coordinator of a basic to moderately complex clinical research studyResponsible for managing and recording all phases of study protocol as required by the sponsoring agency to ensure complianceMay be responsible for multiple research studies simultaneously
Job seniority: associate level
Responsibilities
• Implements and manages all phases of study/protocol• Ensures compliance with protocol guidelines and requirements of regulatory agencies• Recruits and enrolls study participants• Establishes record-keeping systems• Analyzes, investigates and reports adverse events• Resolves protocol management issues and recommends corrective action• Serves as liaison with funding or sponsoring agency• Develops informed consent packets for study participants• Administers/scores tests and/or evaluates all lab and clinical assessments• Collects clinical data under clinical research protocols
Requirements
• Experience in clinical research support or other relevant work experience• Working knowledge of computer programs and systems• Communication, organizational, and interpersonal skills• Bachelor's degree• Basic Life Support certification• Ability to work 40 scheduled hours per week
Benefits
• Up to 22 days of vacation, 10 recognized holidays, and sick time• Competitive health insurance packages• Free Metro transit U-Pass for eligible employees• Forgivable home loan for eligible neighborhoods• Defined contribution Retirement Savings Plan• Wellness challenges, annual health screenings, mental health resources, mindfulness programs and courses, employee assistance program• 4 weeks of caregiver leave for bonding with a new child• Tuition coverage for employees and their families• Other policies and detailed benefits available on the website