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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.
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  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).
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Jobs or company...

Senior Clinical Research Associate (Remote)

Salary undisclosed

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Job Description: Contract Clinical Research Associate (CRA) – Cardiology Exp is a must

Position Overview:

We are seeking a Contract Clinical Research Associate (CRA) specializing in cardiology trials to join our dynamic research team. The ideal candidate will have a strong background in cardiology studies, ensuring compliance with regulatory requirements and contributing to the successful execution of clinical trials.

Key Responsibilities:

  • Site Management: Conduct on-site monitoring visits to assess compliance with study protocols and regulatory guidelines.
  • Data Review: Review and verify the accuracy and integrity of clinical trial data, ensuring timely data entry and resolution of queries.
  • Regulatory Compliance: Ensure all trial activities comply with FDA regulations, ICH guidelines, and institutional policies.
  • Training and Support: Provide training and support to site personnel on study protocols and procedures.
  • Documentation: Maintain comprehensive records of monitoring activities, site communications, and study-related documentation.

Qualifications:

  • Bachelor's degree in life sciences or a related field.
  • Minimum of 5 years of experience as a CRA, with a focus on cardiology trials preferred.
  • Strong understanding of clinical trial processes, regulatory requirements, and Good Clinical Practice (GCP).
  • Excellent communication and organizational skills.

Contract Details:

  • Type: Full-time, 10-month contract
  • Location: Remote monitoring
  • If you are passionate about advancing cardiology research and meet the qualifications, we invite you to apply!
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