Imaging Research Associate

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Clario

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Cardiac Solutions • Medical Imaging • eCOA • Respiratory Solutions • Precision Motion

1001 - 5000

💰 Private Equity Round on 2019-10

Description

• Coordinates all site and operational activities, from study start to study close, to ensure the timely delivery of high quality service deliverables for assigned studies. • Assist in preparation and reproduction of study materials during study start-up phase of clinical trials. • Follow up with outstanding documentations from clinical sites 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 the monitoring and resolution of data discrepancies resulting from discrepancy listings generated from clinical data management. • Manage site communications, generate site and patient reports and queries, and verify reports prior to distribution to clinical sites and sponsors. • Investigate and complete logistical edit checks. • Report issues found with study systems (i.e. study database, reading analysis system). • Perform day to day IQC activities including coordinating, requesting, tracking and processing of IQC data. • Ensure IQC data is collected and maintained according to applicable SOPs and/or study protocol requirements. • Communicate with Clario clinical study team and/or sponsor regarding deliverables. • Participate in project meetings, conference calls, and training calls. • Maintain client (internal and external) satisfaction by responding to inquiries in a professional, courteous and timely manner.

Requirements

• High School Graduate or Associate/Bachelor's Degree in bioscience, computer science, information technology or related field preferred • Familiarity with PC-based computers and standard software packages including e-mail, word processors, Excel spreadsheets and databases. • Knowledge of the drug development/clinical trials process/basic clinical research and/or experience working in a pharmaceutical environment preferred • Knowledge of “good clinical practices” preferred • Familiarity with network navigation and file saving conventions, including moving/copying files and folders • Ability to work in group setting and independently; ability to adjust to changing priorities • Excellent attention to detail and orientation toward meticulous work • Strong interpersonal and communication skills, both verbal and written • Ability to provide and maintain a professional and positive attitude • Leadership skills. • Self-motivated with ability to work in teams with minimal supervision, with aggressive deadlines • Strong documentation and organizational skills • Goal oriented

Benefits

• Competitive compensation • Medical, dental, and vision insurance beginning Day 1 of employment • Flexible work schedules • Attractive PTO plan • Engaging employee programs • Remote working