Scientific Writer

Vibrent Health, a rapidly growing health-tech startup, is looking for a Scientific Writer with a strong understanding of digital technologies, digital informatics, and epidemiology.

As a Vibrent Health Scientific Writer you will be responsible for writing and publishing articles, research papers, and other relevant formal scientific communications on our behalf. You will create comprehensive reports, utilizing formal evidence (including qualitative data,) to be disseminated to peer-reviewed journals and other academic/medical platforms. You will also create webinars or other scientific presentations that align with Vibrent Health’s business pillars and strategic initiatives to drive awareness, understanding and action in support of Vibrent’s mission and programs.

To be successful in this role, you must be a highly motivated, creative individual with experience in delivering high-quality, relevant, and impactful publications. This role will work closely with internal colleagues and external collaborators to translate their initiatives and work into externally relevant publications.

Please note that candidates will be requested to provide 3 writing samples prior to consideration for interview.

This role will be brought on board for a 6-month initial engagement with potential 30-day extensions.

Vibrent Health is a "remote first" team. You will be equipped to work remotely (based in the US,) on a team that is fully remote.
Expectations/ Scope of Role

Develop working knowledge of Vibrent Health’s digital technologies and informatics.
Review and disseminate information from study protocols, questionnaires, digital surveys, data analytics, case report forms, and clinical study reports.
Generate scientific materials for external and internal communication/ clinical evidence dissemination, including (at a minimum): publications for peer-review submission, posters and/or oral presentations that are utilized at academic meetings, study abstracts, study outcome summaries for use in training presentations, and white papers.
Conduct literature reviews on relevant topics and develop citation libraries of relevant publications.
Coordinate review and contributions of content from internal and external colleagues and communicate effectively across a diverse global network of businesses.
Maintain an organized collection of clinical and scientific resources to support regulatory, research and marketing initiatives.
Receive edits and critical review of scientific/presentation materials from peers and incorporate into future iterations.
Work collaboratively with departments across the organization to maximize the impact of strategic initiatives.
Consistently deliver materials of high-quality that withstand critical review, including peer (scientific, regulatory, marketing) review, as well as review/ audit from regulatory or notified bodies.
Coordinates the submission, review, revision, quality control, quality assurance, electronic publishing, and approval of manuscripts, abstracts, and other documents.

Requirements

Bachelor’s degree required, preference given to candidates with training/experience in journalism, communications, and/or biomedical and clinical research.
Demonstrated experience in publishing peer-reviewed research articles.
Must be knowledgeable in interpreting data analytics, data modeling, and data programming.
Excellent writing, interpersonal, and oral communication skills with proven ability to present, write, edit, and organize thoughts in a clear, concise, and well-organized manner.
Ability to understand materials of moderate complexity and synthesize across multiple sources to produce materials for diverse audiences.
Ability to change voice and writing style to fit a particular audience and purpose.
Ability to apply analytical skills to effectively summarize, communicate, and present clinical research outcomes.
Ability to manage and prioritize multiple deadlines.