Medical Writer IV

Our client, a leading organization in the medical device industry, is seeking a Medical Writer IV to join their team. As a Medical Writer IV, you will be part of the Regulatory Clinical Evaluation department supporting clinical evaluation reporting and documentation. The ideal candidate will demonstrate strong communication skills, attention to detail, and a collaborative mindset, which will align successfully in the organization.

Job Title: Medical Writer IV

Location: On-site at our Maple Grove, MN, Plano, TX, or Santa Clara, CA locations. Please note this position is not remote.

Pay Range: $63/hr w2

What's the Job?

• Author and contribute to Clinical Evaluation reporting deliverables including Clinical Evaluation Plans/Reports, SSCPs, Regulatory Responses, and related documentation.
• Evaluate and summarize clinical evidence from various sources such as clinical investigations, literature, and post-market surveillance.
• Collaborate with cross-functional teams to support CER projects and ensure alignment with regulatory requirements.
• Review and ensure the quality, accuracy, and compliance of clinical evaluation documents and related materials.
• Assist in preparing documents for regulatory submissions and respond to complex queries from stakeholders and notified bodies.

What's Needed?

• Bachelor's Degree or equivalent education and work experience in a relevant field.
• 6-8 years of medical or scientific writing experience in the medical device, pharmaceutical, or clinical research industry.
• Experience with MDR compliant CERs, CEPs, and SSCPs for Class III medical devices.
• Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).
• Strong analytical skills, attention to detail, and ability to manage complex tasks effectively.

What's in it for me?

• Opportunity to work on impactful medical device projects in a dynamic environment.
• Collaborative team culture that values innovation and professional growth.
• On-site work with potential for career development within a global organization.
• Engagement in regulatory activities that contribute to patient safety and product excellence.
• Supportive work environment committed to diversity and inclusion.

Upon completion of waiting period, consultants are eligible for:

• Medical and Prescription Drug Plans
• Dental Plan
• Vision Plan
• 401(k), Plus Match
• Weekly Pay

If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!

About ManpowerGroup, Parent Company of: Manpower, Experis and Talent Solutions.

Experis® is a global leader in technology services and part of the ManpowerGroup® (NYSE: MAN) family of brands. We connect skilled technology professionals with meaningful opportunities where they can grow their careers, expand their expertise and make a real impact. Guided by the belief that it takes Human Ingenuity to unlock the true potential of technology, Experis helps people gain experience with leading organizations, build sought-after skills and take the next step toward a brighter future. Backed by ManpowerGroup's 75+ years of workforce expertise and global reach across more than 70 countries and territories, Experis brings the scale, insight and opportunity to help people and businesses thrive. ManpowerGroup is consistently recognized for its commitment to inclusion, ethics and responsible business, including being named one of the World's Most Ethical Companies. Learn more at Experis.com.