Full-Time

Scientific Writer

Posted on 11/1/2025

University of Miami

University of Miami

No salary listed

Company Does Not Provide H1B Sponsorship

Miami, FL, USA

In Person

Category
Content & Writing (2)
,
Required Skills
SAS
R
Requirements
  • Ability to edit and format grant proposals and scientific documents ensuring readability and conformance to submission requirements.
  • Experience communicating with principal investigators and senior leadership authors to ensure accuracy and clarity of documents.
  • Familiarity with regulatory submissions processes and policies; ability to ensure documents conform with applicable regulations, guidelines, and policies; notify PI or director as required and suggest corrections.
  • Experience conducting literature reviews and editing clinical/statistical reports and study protocols.
  • Ability to summarize data from clinical studies for submission to governmental/regulatory agencies.
  • Proficiency with statistical software such as R, SPSS, or SAS and with data visualization to present research data clearly to stakeholders.
  • Ability to design and execute data management plans ensuring data integrity, quality control, and regulatory/ethical compliance.
  • Experience collaborating with research teams to identify data analysis needs and implement innovative approaches to solving scientific and clinical questions.
  • Experience compiling and integrating data from multiple sources for comprehensive analysis and aiding in preparation of scientific manuscripts, presentations, and regulatory submissions.
Responsibilities
  • Creates, implements, and maintains competitive application templates for grant proposals.
  • Formats substantive copy and scientific editing, proofreading, and finalizing documents as required and requested.
  • Ensures readability, clarity, consistency, and conformance to applicable submissions requirements.
  • Reviews and ensures document language is scientifically/medically correct, responsive to document requirements, consistent, and justifiable; notifies appropriate PI or leader and suggestion alternative language, as required.
  • Communicates (telephone, email, meetings) with principal investigator and key senior leadership authors as necessary to ensure the accuracy and clarity of documents; meets both internal and sponsor submission deadlines.
  • Researches, composes and edits clinical/statistical reports and study protocols.
  • Summarizes data from clinical studies for submission to appropriate governmental/regulatory agencies.
  • Edits all extramurally funded proposals for grammar, readability, clarity, consistency, and conformance with all applicable requirements.
  • Works closely with presenters in the development of scientific presentations, ensuring accuracy and adherence to length and time allowed for presentation.
  • Ensures that documents conform with all applicable regulations, current guidelines, and policies; inform appropriate PI or director as required and suggest appropriate correction.
  • Obtains and maintains the documentation for any required copyright transfers, conflict of interest statements, or other publisher-specific requirements.
  • Tracks progress and responds to publication queries, as appropriate; Adheres to University and unit-level policies and procedures and safeguards University assets.
  • Desirable: None
Desired Qualifications
  • None

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INACTIVE