Medical Affairs Senior Medical Writer

Sandy, UT Open
MILLENNIUMSOFT is looking for Medical Affairs Senior Medical Writer in Sandy, UT. This local job opportunity with ID 3662914565 is live since 2026-05-04 14:28:34.

Position: Medical Affairs Senior Medical Writer

Location: Sandy, UT

Duration: 12+ Months Contract

Total Hours/week: 40.00

Description:

Job Description Summary:
Medical Affairs is responsible for ensuring the safety and efficacy of Medication Delivery Solutions (MDS) products worldwide. The Medical Writer will support this mission by assisting with and / or compiling, reviewing and summarizing, available data to access the safety and efficacy of MDS products worldwide.

Job Description:
The Medical Affairs Medical Writer will combine their knowledge of science with their understanding of research and writing to present information effectively and with clarity. The Medical Writer will focus on scientific medical writing to prepare documents – clinical evaluation plans (CEPs) and clinical evaluation reports (CERs) – for submission to regulatory bodies. The Medical writer will collaborate with other functions and with the Senior Medical Writer as necessary to ensure accurate and timely completion and review of clinical documents for regulatory submissions.


Education & Experience:
• Minimum of a Bachelor’s Degree required.
• Experience in a relevant Medical Device Industry required
• Minimum of 2-3 years writing experience within the Medical Device Industry.
• Certification through the American Medical Writing Association (AMWA) or other relevant association is preferred.

Skills:
• Ability to write with scientific accuracy and to compile, write, edit and format documents for submission to regulatory agencies. (Writing samples required)
• Experience in conducting literature searches required
• Ability to develop and conduct comprehensive literature searches i.e., interpret / summarize / synthesize relevant literature)
• Understanding of MEDDEV 2.7/1 rev4 guidelines and the MDR regulations related to clinical evaluation reports preferred.
• Ability to ensure that all deliverables are in accordance with applicable regulations, standards, and guidelines
• Excellent written and verbal communication skills.
• Superior attention to detail.
• Proficiency in MS Office with expertise in Microsoft Word with a special focus on word processing, use of templates, and formatting. Working knowledge of Excel.
• Proficiency with a PC
• Excellent time management skills, and ability to meet deadlines
• Working knowledge of statistical concepts and techniques.
• Experience in working with collaborative, cross-functional teams.
• Ability to function well both individually and as part of a team.
• Experience in working with collaborative, cross-functional teams.
• Ability to function well both individually and as part of a team.
• Experience in working with collaborative, cross-functional teams.
• Ability to function well both individually and as part of a team.
• Experience in working with collaborative, cross functional teams
• Ability to function well both individually and as part of a team

Required Skills