Job Description

Job Description

Job Description

Job Title: Medical Writer
Client: Medical Device Manufacturing Company
Duration: 12 Months
Location: Maple Grove, MN, 55311

**Mandatory- Must be US Citizen or Green Card Holder Only

Key Words:

• CER (Clinical Evaluation Review/Report) Writing
• MDR (Medical Device Regulations)
• EU (European Union)
• Literature Review (e.g., PubMed)

Responsibilities:

• Write and review scientific manuscripts, congress abstracts, and scientific meeting presentations aligned with journal and congress guidelines.
• Prepare clinical content for study investigator meetings, interim data analyses, and other internal/external meetings related to clinical studies.
• Create symposia (non-CME), speaker decks, post-meeting slide decks, topical slide decks, and other Professional Education modules as needed.
• Collaborate extensively with internal medical leadership, clinical research scientists, clinical trial managers, medical affairs managers, statisticians, and other medical writers as part of publication teams.
• Develop partnerships with study investigators, external authors, and interact externally with journals, conference organizers, and freelance/contract medical writers.
• Ensure clinical data is represented accurately in published literature, slide sets, and other materials.
• Lead and organize document production meetings and related activities.
• Review documents related to clinical evidence for proper evaluation and presentation of data, methodology, and interpretation.

Required Qualifications:

• Degree in Life Sciences (Advanced degree preferred).
• Experience in Medical Device or Pharmaceutical Industry with a focus on Medical Writing or Clinical Research.
• Extensive experience in writing, editing, and submitting publications to journals and congresses.

Preferred Qualifications:

• 5-7 years of relevant experience.
• Therapeutic area knowledge in peripheral interventions is desired.
• Excellent written, analytical, verbal, and communication skills.
• Ability to manage multiple projects independently and meet deliverables on time.
• Capable of working effectively in a matrix environment.
• Ability to develop strategic solutions to significant business issues.
• Commitment to patient safety and product quality by adhering to the Quality Policy and documented quality processes and procedures.

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