Epicareer Might not Working Properly
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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.
Visit Site here
  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.
Visit Site here
  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 Research Associate

Salary undisclosed
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Original
Simplified

Sr. Clinical Research Associate

12-month contract

Onsite in Sunnyvale, CA

Responsibilities

  • Support the successful execution of clinical studies by contributing to study design, documentation, and overall management.
  • Lead and manage site start-up and activation processes, including regulatory document preparation, IRB/EC submissions, and clinical trial agreements.
  • Conduct monitoring visits (qualification, initiation, interim, and close-out) and ensure protocol and regulatory compliance through source data verification and study oversight.
  • Serve as the primary liaison for clinical sites, overseeing data entry, investigational device tracking, and issue resolution.
  • Maintain and manage study documentation, including Trial Master File (TMF), clinical trial management systems (CTMS), and site payments.

Qualifications

  • Experience implementing and managing medical device clinical trials.
  • In-depth knowledge of ISO 14155, 21 CFR Part 11, 50, 54, 812, and ICH/GCP regulations.
  • Proficiency in developing study documents (protocols, informed consent forms, CRFs/eCRFs, monitoring plans).
  • Experience with clinical research budgeting and contract negotiation.
  • Proficiency with Microsoft Office Suite, PDF applications, and Electronic Data Capture (EDC) systems.
  • Experience with Clinical Trial Management Systems (CTMS).
  • Prior experience in protocol and clinical section writing for regulatory submissions.
  • Experience in medical device industry is required.

Sr. Clinical Research Associate

12-month contract

Onsite in Sunnyvale, CA

Responsibilities

  • Support the successful execution of clinical studies by contributing to study design, documentation, and overall management.
  • Lead and manage site start-up and activation processes, including regulatory document preparation, IRB/EC submissions, and clinical trial agreements.
  • Conduct monitoring visits (qualification, initiation, interim, and close-out) and ensure protocol and regulatory compliance through source data verification and study oversight.
  • Serve as the primary liaison for clinical sites, overseeing data entry, investigational device tracking, and issue resolution.
  • Maintain and manage study documentation, including Trial Master File (TMF), clinical trial management systems (CTMS), and site payments.

Qualifications

  • Experience implementing and managing medical device clinical trials.
  • In-depth knowledge of ISO 14155, 21 CFR Part 11, 50, 54, 812, and ICH/GCP regulations.
  • Proficiency in developing study documents (protocols, informed consent forms, CRFs/eCRFs, monitoring plans).
  • Experience with clinical research budgeting and contract negotiation.
  • Proficiency with Microsoft Office Suite, PDF applications, and Electronic Data Capture (EDC) systems.
  • Experience with Clinical Trial Management Systems (CTMS).
  • Prior experience in protocol and clinical section writing for regulatory submissions.
  • Experience in medical device industry is required.