What We Offer

• Competitive compensation

• Private health insurance

• Engaging employee programs

• Flexible work schedules

• Attractive PTO plan

• Flex workspace

What You’ll Be Doing

• Coordinate site and operational activities throughout the study lifecycle

• Assist in preparation and reproduction of study materials during start-up phase

• Follow up on outstanding documentation to complete site qualification

• Schedule logistical and technical trainings with site personnel

• Create test run requests for sites submitting digital data

• Review, process, track, and monitor all study-related data received from sites

• Assist in monitoring and resolving data discrepancies from clinical data management

• Manage site communications, generate reports and queries, and verify accuracy before distribution

• Investigate and complete logistical edit checks

• Report issues found with study systems (e.g., study database, reading analysis system)

• Perform day-to-day IQC activities including coordinating, requesting, tracking, and processing IQC data

• Ensure IQC data is collected and maintained according to SOPs and study protocol requirements

• Communicate with clinical study teams and sponsors regarding deliverables

• Maintain study database and prepare BMD Scan Review Forms

• Support Project Managers with project administration, tracking, and reporting

• Participate in project meetings, conference calls, and training sessions

What We Look For

• High school diploma or Associate/Bachelor’s degree in bioscience, computer science, information technology, or related field preferred

• Familiarity with PC-based computers and standard software packages (Word, Excel, email, databases)

• Knowledge of clinical trials process and good clinical practices preferred

• Ability to navigate networks and manage files effectively

• Strong attention to detail and organizational skills

• Excellent verbal and written communication skills

• Ability to work independently and in a team environment with changing priorities

• Professional, positive attitude and strong interpersonal skills

• Leadership qualities and ability to meet aggressive deadlines

At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.