Medical Writer

August 17

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Logo of Alimentiv

Alimentiv

Clinical Trials Design • Planning • Safety Management • Custom Services • Study Management

201 - 500

Description

• Provide scientific writing services to Sponsors, Clinical Research Scientists, Academic partners, and/or the Corporation • Lead the content planning and production of regulatory documents that align with established standards and guidelines. • Work with authors/technical specialists to coordinate the completion of specialized content, to translate, write, edit and/or proof data and content for publication into finished documents appropriate for the stated audience. • Regularly track timelines and provide progress reports to stakeholder(s). • Participate in quality control review for documents written by other authors when requested. • Upon request, assist in the development of sales, marketing, and promotional materials. • Will be required to translate complex scientific information, theories, practices and/or findings into clear, concise, and accurate language that can be understood by potential clients, sponsors and/or the general public. • Develop lay summaries of study results, protocol synopses, or other study materials as required. • Act as primary contact and liaison with external publication executives, illustrators, designers, and editors representing the Scientists/Investigators, Sponsors and/or the corporation with external specialists.

Requirements

• Minimum of an undergraduate degree (advanced degrees preferred) and 3-5 years of relevant experience in medical writing • Previous experience with CSRs, IBs, Protocols, and ICFs. • Knowledge of ICH-GCP • Ability to adapt to shifting priorities and assignments • Highly refined written and oral communication skills • Demonstrated ability to work with diplomacy and tact • Previous experience/knowledge of Gastroenterology is an asset • Familiarity with AMA Style Guide is an asset

Benefits

• Accommodations for job applicants with disabilities are available

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