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.

#ZR

Job Tags

Contract work, Interim role, Freelance

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