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