Associate Medical Writer

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Associate Medical Writer, United Kingdom (Remote)

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Job Category:

-

EU work permit required:

Yes

Job Reference:

4dc33897eddb

Job Views:

9

Posted:

26.04.2025

Expiry Date:

10.06.2025

Job Description:

At the forefront of clinical research innovation, our esteemed medical imaging core lab is searching for an Associate Medical Writer who embodies precision, passion, and a penchant for progress. Your role will be pivotal in shaping the narrative of clinical trials, ensuring the integrity and clarity of medical communications, and ultimately, influencing the lives of patients worldwide.

What we offer

• Competitive compensation
• Attractive benefits (security, flexibility, support, and well-being)
• Remote working with full technology setup

What you'll be doing

1. Performing study start-up responsibilities such as entering new studies into the MedComm database, creating study-specific folders, organizing documents, requesting signed protocols, and notifying project teams.
2. Reviewing study protocols related to imaging requirements, schedules, and windows.
3. Creating, modifying, and finalizing site manuals, fillable forms, and labels.
4. Preparing compliance reports like PAIFs, NTFs, Corrections, and ToO.
5. Developing source documents and eCRFs for outside reads.
6. Creating and reviewing MedComm meeting minutes.
7. Participating in meetings related to study start-up documents.
8. Maintaining MedComm web pages for internal use.
9. Managing project close-outs and updating SOPs and training modules.
10. Reviewing and updating reader training packages.
11. Managing the clinical study document development process, including creating, modifying, and attaching CRs.
12. Updating MedComm databases and tracking spreadsheets.
13. Providing guidance to project teams and updating document templates as needed.
14. Creating final effective documents.

What we look for

• Bachelor’s Degree in Life or Physical Sciences preferred.
• 1+ years medical writing experience preferred but not required.
• 2+ years experience in pharmaceutical/clinical/imaging research preferred.
• Proficiency in medical, pharmaceutical, regulatory, clinical writing.
• Proficiency in MS Office Suite.
• Understanding of medical and clinical trial terminology desired.

At Clario, we put people first, always. We are committed to diversity, inclusion, and making a positive impact. We encourage passionate candidates to apply and join us in transforming lives.