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.
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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...

Medical Affairs Content Specialist

Salary undisclosed

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Responsibilities:

  • Excellent employment opportunity for a Clinical Trial Education and Literature Review Specialist in the Santa Monica, CA area.
  • Fully remote role. EST is preferred
  • We are seeking a detail-oriented and analytical Clinical Trial Education and Literature Review Specialist to support the development and submission of clinical trial education materials to the Promotional Review Committee (PRC).
  • Responsible for conducting comprehensive literature reviews to assess the landscape of new and emerging medical indications.
  • The ideal candidate will work closely with cross-functional teams, including medical affairs, regulatory, and marketing, to ensure that all materials are accurate, compliant, and aligned with the latest medical research.
  • Develop, organize, and submit clinical trial education materials to the Promotional Review Committee (PRC) for review and approval, ensuring compliance with regulatory and company guidelines.
  • Provide ongoing support during the PRC review process, addressing feedback, revising materials, and ensuring timely approval.
  • Conduct thorough literature reviews to gather and analyze data on new medical indications, treatment trends, and advancements in the field.
  • Collaborate with cross-functional teams (Clinical Development, Medical Affairs, Regulatory, Marketing, etc.) to ensure educational materials align with clinical trial objectives and reflect the latest medical information.
  • Monitor and stay current on industry trends, new therapies, and scientific advancements that may impact clinical trial materials or strategic positioning.
  • Synthesize complex medical and scientific information into clear, concise educational content for internal and external audiences.
  • Assist in the development of communication strategies that effectively educate healthcare professionals about clinical trials, investigational products, and new medical indications.
  • Ensure all educational materials are updated and consistent with the latest clinical trial data and regulatory requirements.
  • Maintain a comprehensive database of clinical trial education materials and literature review findings for easy access and future reference.

Experience:

  • Bachelor’s degree in Life Sciences, Clinical Research, Healthcare, or a related field (Advanced degree preferred).
  • 2-4 years of experience in Clinical Research, Medical Affairs, Regulatory Affairs, or Medical Communications.
  • Experience preparing materials for Promotional Review Committees or similar review bodies.
  • Strong understanding of clinical trial processes, regulatory requirements, and promotional guidelines (e.g., FDA, EMA).
  • Demonstrated experience conducting literature reviews, including the ability to analyze,
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