Accordance Search Group Hiring for Clinical Research Associate at Atlanta, GA Full Time

The US Pharma Clinical Specialist is responsible for setting-up and executing our range of clinical trial services to pharmaceutical companies, Biotech’s, and CROs who are involved in the development of treatment for chronic liver diseases.

Location: US, with ability to work with European hours/time zone

Job Responsibilities: The specific duties of the US Pharma Clinical Specialist include but are not limited to:

• Support the Pharma team in delivering our FibroScan trial services to Sponsor and CRO customers: site qualification, device deployment, on-site certification, pre-trial data quality control, in-trial data quality control…
• Lead and document FibroScan site qualification for our Sponsor and CRO customers, incl. FibroScan capabilities assessment, interactions with PI and sites coordinators, recommendations and data upload
• Coordinate FibroScan on-site certification, pre-trial and in-trial quality control: manage interactions between Clinical Sites and Echosens teams, coordinate activities from Clinical Application Specialists & Trainers, maintain corresponding sponsor-facing, site-facing and Echosens internal documentation
• Contribute as a QC expert to pre-trial quality control and in-trial quality control
• Monitor FibroScan capabilities of our Pharma and CRO customers during clinical trials: training, probe calibration, service needs…
• Lead documentation of our Pharma and CRO customers trials on SFDC, incl. creation and maintenance of Clinical Studies, Clinical Sites and site contacts to capture and monitor all FibroScan-related information in supported clinical trials
• Conduct special projects as necessary upon Sponsor request (SmartEraser, etc.)
• Lead and interact with our Pharma and CRO customers during sponsor calls
• Interact with their Clinical Sites via email or phone, if needed

Qualifications

• Minimum of a Bachelor’s Degree
• Minimum of three (3) years of successful experience as a Clinical Research Associate in a Sponsor, CRO or Imaging Vendor
• Preferred experience in managing imaging vendors or medical device/diagnostic provider in the context of clinical trials
• Must be able to meet all hospital credentialing requirements, including but not limited to, background check, drug screen and certain immunizations
• Must be insurable and maintain a valid driver’s license
• Must be willing and able to travel (by automobile or air, day trips and overnight stays) approximately 40%

Benefits:

• $700/mth car allowance, phone, internet ($40/mth), computer, ipad
• 401K and 4% match, starts immediately
• Medical benefits, starts immediately
• 15 days’ vacation plus holidays

Powered by JazzHR

1xNC8XeHKe