Description

Medical Writer II-Sr Medical Writer

Duration: 6-12 months from the start date of the worker with possible conversion/extension

Location: Maple Grove MN -Onsite Role

Schedule: Possibility to be flexible after initial training period, so the person could have a hybrid schedule thereafter and this will be worked out with the HM

• The Sr. Medical Writer on our Regulatory Clinical Evaluation team provides technical and strategic writing expertise throughout the product development and life cycle process.
• Daily activities are related to authoring Clinical Evaluation Reporting documents for the Neuromodulation, CAHF and Vascular products.
• Experience in clinical study management and design, medical, or scientific writing, and/or quality engineering/risk management and strong written and verbal communication skills are needed.

Top 3 Skills or Any Specific type of Experience you are looking for:

• Experience writing Medical Device MDR compliant CERs, CEPs and SSCPs
• Microsoft Office proficiency
• Structural Heart, Neuromodulation, or other medical device experience such as Clinical Study Management

EDUCATION AND EXPERIENCE

Required

• Bachelor’s Degree or an equivalent combination of education and work experience
• 4-6 years of medical writing experience in the medical or pharmaceutical industry or 7+ years general technical writing experience required
• Experience may include writing experience in a medical, pharmaceutical, medical device, clinical research, medical or research industry , or combination of these skills

Preferred

• Biomedical, sciences, medicine or similar health related discipline preferred
• CER writing experience preferred
• Excellent written and verbal communication skills
• Experience with collaborative, cross-functional teams.
• Excellent analytical skills and ability to manage complex tasks and manage time