P

Precision AQ

Data-driven drug access and launches

Medical Writer - Medical Communications

Technical WritingConfirmed live in the last 24 hours
Full-timeRemote in USARemote

About the Job

Requirements

  • A doctoral-level degree in life sciences (PhD, PharmD, MD, or equivalent) is required.
  • Strong interest in medical writing and scientific communication is required.
  • The candidate must be detail-oriented and have strong written and verbal communication skills.
  • The candidate must have strong time-management skills and be able to balance work on multiple projects.
  • Familiarity with Microsoft Word, PowerPoint, Excel, Teams, OneNote, Outlook, and Adobe Acrobat is required.
  • Familiarity with or willingness to learn AMA style and reference tools such as EndNote is required.
  • Candidates must be legally authorized to work in the country of employment without employer sponsorship.

Responsibilities

  • Draft and revise scientific content, including slide decks, manuscripts, training materials, and other deliverables, with supervision aligned to experience.
  • Interpret clinical and preclinical data and translate findings into clear, accurate written content and visual representations.
  • Learn, apply, and consistently follow AMA style and client-specific guidelines.
  • Conduct literature searches and organize references using appropriate systems and tools.
  • Participate in internal and client meetings to support content discussions.
  • Listen during meetings and capture accurate notes and action items as needed.
  • Incorporate direct feedback from internal and external reviewers accurately and efficiently.
  • Communicate with internal teams and external stakeholders.
  • Work with the manager to maintain an 85% billable utilization goal.
  • Learn and follow team standards and processes, including becoming proficient in software or other technical tools required for project completion.
  • Track tasks, timelines, and file handoffs using appropriate tools, including Workfront, SharePoint, and Microsoft Teams, with guidance as needed.
  • Track and report time accurately.
  • Build efficiency and deliver work within budgeted hours.
  • Collaborate with the team to prepare materials for regulatory and editorial review.
  • Review and follow standard operating procedures with the manager, asking questions to understand processes and rationale.
  • Collaborate with team members and contribute to a professional and reliable working environment.
  • Develop an understanding of team roles and responsibilities and collaborate accordingly.
  • Receive feedback and work with the manager or Scientific Director on skill refinement.
  • Prepare for time off using planning templates and ensure appropriate delegation of access as responsibilities increase.

Desired Qualifications

  • Prior medical writing experience is beneficial but not required; the level of independence will align with experience.

About the Company

Precision AQ

Data-driven drug access and launches

Precision AQ helps pharmaceutical companies get FDA-approved medicines to patients by using data, evidence, and market insights to shape access and launches. Its services combine medical science, commercial strategy, and technology development to create new pathways for drug availability and timely delivery. The company partners with drug makers to plan launches and expansion, using analytical and creative approaches to make medicines reachable and effective in real-world settings. Unlike firms that focus only on science or marketing, Precision AQ blends data-driven insights with strategic execution across development and commercialization to accelerate patient access. The goal is to raise standards in healthcare accessibility and impact by getting the right medicines to the right patients faster.

Company size
501-1,000
Company stage
Not listed
Total funding
Not listed
Headquarters
New York City, New York
Founded
Not listed

Recently Posted Jobs

Explore more opportunities at Precision AQ

See more jobs