Clinical Research Associate

Ideal Candidate :

• Independent and ability to manage multiple projects at the same time
• Detail-oriented and ability to handle fast paced environment
• Strong communication skills needed will be communicating with sponsors and healthcare providers
• Ability to be professional and communicate with external customers
• Experience with salesforce and manage trackers is preferrable

Location : Remote but NE region is preferred for easier travel. Will also be working with team in Paris and will need to accommodate calls with Paris timezone

Travel : Will be around 40% in the beginning for training. (no international travel) Will be going to sites / training for studies.

After training, travel will be minimal and will more as needed . HQ is in Boston and there will be 1 week of training in Boston

Compensation :

• $700 / mth car allowance, phone, internet ($40 / mth), computer, ipad
• 401K and 5% match, starts immediately
• Medical benefits, starts immediately
• 15 days’ vacation plus holidays

Position Summary

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.

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 company teams, coordinate activities from Clinical Application Specialists & Trainers, maintain corresponding sponsor-facing, site-facing and company 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
6 hours ago