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Clinical Research Associate
$62k-82k (estimate)
Full Time 1 Month Ago
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Accordance Search Group is Hiring a Remote Clinical Research Associate

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.
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

Job Summary

JOB TYPE

Full Time

SALARY

$62k-82k (estimate)

POST DATE

03/25/2024

EXPIRATION DATE

06/20/2024

WEBSITE

accordancesearch.com

SIZE

<25

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The job skills required for Clinical Research Associate include Clinical Research, Clinical Trial, etc. Having related job skills and expertise will give you an advantage when applying to be a Clinical Research Associate. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Clinical Research Associate. Select any job title you are interested in and start to search job requirements.

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The following is the career advancement route for Clinical Research Associate positions, which can be used as a reference in future career path planning. As a Clinical Research Associate, it can be promoted into senior positions as a Scientist - Clinical Research that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Research Associate. You can explore the career advancement for a Clinical Research Associate below and select your interested title to get hiring information.

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