Senior Medical Writer – Oncology

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timePosted 11 days ago location United States salarySalary undisclosed

Job Description

Sr Medical Writer- Home-based – Oncology

  • Job Locations: (All) | US-Remote
  • ID: 2020-63525

Overview

Researches, writes, and edits clinical and regulatory documents by applying functional expertise and clinical drug development knowledge. Writes clear and concise documents, including study reports, protocols, investigator brochures, summary documents, and other scientific documents. Exhibits excellent written and oral communication and presentation skills. Demonstrates technical expertise and background in the use of medical writing templates and software (eg, PleaseReview, Documentum-based platforms, etc.).

Responsibilities

Responsibilities

  • Manages all aspects of the medical writing function.
  • Writes and reviews clinical study reports, protocols, and other clinical/regulatory documents.
  • Contributes to clinical protocol development for first-in-human oncology studies.
  • Demonstrates technical expertise and background in the use of medical writing templates and software (eg, PleaseReview, Documentum-based platforms, etc.).
  • Writes clear and concise documents, including study reports, protocols, investigator brochures, summary documents, and other scientific documents
  • Drive the document preparation process, receive and review primary statistical output, draft and distribute documents for review, and incorporate/resolve comments with all reviewers.
  • Acts as a lead medical writer on complex programs and numerous individual studies.
  • Provides scientific and medical writing consultancy to project teams, as requested.

Qualifications

Qualifications

  • Advanced degree in a relevant scientific/clinical/regulatory field preferred
  • At least 5 years of experience in a lead oncology medical writing role in the pharmaceutical/CRO industry. *Note: Early development oncology experience is preferred.
  • Excellent writing skills.
  • Ability to understand and interpret clinical and scientific data; ability to present results in an understandable manner to a variety of audiences.
  • Knowledge of current requirements and guidelines applicable to submission documents
  • Excellent interpersonal and oral communication skills.
  • Strong knowledge of MS Word, Excel, PowerPoint, and Outlook
  • Ability to prioritize multiple projects
  • To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.

PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.