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Please Turn on your JavaScript

Epicareer might not working properly because your browser javascript is turned off.

What is JavaScript?

JavaScript is like the magic behind making websites interactive. Basically, it makes Epicareer more enjoyable and engaging.
How do i turn this on?
Find tutorial for your browser below :
  1. Make sure the webpage is open.
  2. In the Safari app on your Mac, choose Safari > Preferences, then click Security.
  3. Make sure the Enable JavaScript checkbox is selected.
  4. Click Websites.
  5. On the left, click Content Blockers.
  6. Make sure Off is chosen in the pop-up menu next to the website.
  7. On the left, click Pop-up Windows.
  8. Make sure Allow is chosen in the pop-up menu next to the website.
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  1. Open Chrome on your computer.
  2. Click. then Settings.
  3. Click Privacy and Security.
  4. Click Site settings.
  5. Click JavaScript.
  6. Select Sites can use Javascript.
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  1. If you're running Windows OS, in the Firefox window, click Tools > Options.
  2. Tip: If you're running Mac OS, click the Firefox drop-down list > Preferences.
  3. On the Content tab, click the Enable JavaScript check box.
Visit Site here
  1. Click the "Settings and more" icon at the top right of the Edge browser window.
  2. Click Settings.
  3. From the Settings menu, click Cookies and site permissions.
  4. Scroll down and click on JavaScript.
  5. In the JavaScript window, toggle the slider to "on" or "allowed."
  6. Close the Settings tab.
  7. Refresh the page.
Visit Site here
  1. Go to Settings.
  2. Click Advanced in the left sidebar, and click Privacy & security.
  3. Under Privacy and security, click Site settings.
  4. Click JavaScript.
  5. At the top, turn on or off Allowed (recommended).
Visit Site here
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Jobs or company...

Clinical Data Coordinator

Salary undisclosed

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Job Title: Clinical Data Coordinator

Location: Maple Grove, MN

Duration: 6+ Month W2 Contract

Pay: $36k - 40k/year

Job Summary: Oversee data management activities for clinical studies, ensuring the integrity of study data by entering, reviewing, modifying, reconciling, and organizing data. This role requires working onsite and involves testing and verifying clinical data management systems, managing discrepancies, and complying with FDA regulations.

Key Responsibilities:

  • Data Management:
  • Develop and maintain Case Report Forms and Edit Check specifications
  • Create and update Data Management Plans
  • Perform data quality checks and manage discrepancies (creating, routing, and resolving)
  • Analyze data and prepare reports, with intermediate-level knowledge of Excel functions such as pivot tables, search functions, and XLOOKUP
  • Test database setups and Edit Check programming
  • Handle external data and device reconciliation
  • Participate in Post Market Surveillance reporting as needed
  • Ensure compliance with FDA regulations, ICH guidelines, ISO 14155, and company policies
  • Potential for occasional overtime

Qualifications:

  • Minimum of 2 years in a comparable or closely related clinical research environment. 1 year of experience may be considered if all other requirements are met. Medical device experience is a plus.
  • Proficiency in computer skills, including Excel (pivot tables, search functions, XLOOKUP)
  • Ability to manage multiple projects
  • Experience with clinical databases (Oracle preferred but not required)
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