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Job summary
A leading medical device company is seeking a Medical Writer to develop clinical documents for an innovative project. This role focuses on drafting a Clinical Development Plan and protocols for early feasibility studies. Candidates should have experience with medical device studies and be able to convert complex scientific information into regulatory-ready documents. Candidates based in the U.S. and Europe are encouraged to apply. This is a remote role with an initial contract of 6-12 months.
Qualifications
Experience drafting clinical development plans and early-phase protocols.
Experience with medical device clinical studies.
Familiarity with Early Feasibility Studies and/or First-in-Human trials.
Responsibilities
Draft a comprehensive Clinical Development Plan.
Draft Ex-Vivo protocol for proof-of-concept.
Incorporate SME input and manage document versioning.
Skills
Drafting clinical development plans
Knowledge of medical device clinical studies
Familiarity with Early Feasibility Studies
Translating scientific information
Working under tight timelines
Job description
A leading medical device company is seeking a Medical Writer to develop clinical documents for an innovative project. This role focuses on drafting a Clinical Development Plan and protocols for early feasibility studies. Candidates should have experience with medical device studies and be able to convert complex scientific information into regulatory-ready documents. Candidates based in the U.S. and Europe are encouraged to apply. This is a remote role with an initial contract of 6-12 months.