Medical Writer, Scientific Communications
Posted 2026-05-06
Remote, USA
Full-time
Immediate Start
- Job Description:
- Prepare high-quality abstracts and presentations for submission and presentation at conferences.
- Engage in scientific writing and/or edit manuscripts for submission to peer-reviewed journals to achieve publication goals.
- Ensure scientific communication deliverables are completed in a timely manner.
- Evaluate data and translate information into succinct, scientific summaries.
- Collaborate cross-functionally with clinical, marketing, and creative teams to ensure data dissemination goals and deadlines are met.
- Work with clinical study management and statistics teams to create timelines for completing data dissemination plans related to clinical studies.
- Strong communication with physician authors to achieve deliverables, maintain relationships, and to facilitate overall scientific communication efforts.
- Contribute to the preparation of clinical data for analysis and scientific writing.
- Conduct literature searches for relevant disease states and maintain the clinical literature library.
- Lead cross-functional project reviews and serve as a core team member and subject matter expert on clinical study teams to create timelines for completing medical writing documents.
- Adhere to the Company’s Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures. *
- Understand relevant security, privacy and compliance principles and adhere to the regulations, standards, and procedures that are applicable to the Company. *
- Ensure other members of the department follow the QMS, regulations, standards, and procedures. *
- Perform other work-related duties as assigned.*Indicates an essential function of the role
- Requirements:
- Advanced degree (Master’s, PhD, or MD) with 2+ years of experience as a medical writer in the medical device, biotech, or pharmaceutical industry; or 5+ years of experience as a medical writer in clinical/scientific research, or an equivalent combination of education and experience.
- Experience as a medical writer for cardiovascular clinical trials in the medical device, biotech, or pharmaceutical industries is preferred.
- Demonstrates a diligent approach to work, with a portfolio that showcases outstanding writing skills and a passion for clarity in written expression.
- Team player with excellent organizational skills and the ability to prioritize assignments and manage multiple projects simultaneously, both independently and collaboratively.
- Proficient in Microsoft Office 365.
- Familiarity with laws, regulations, standards, and guidance governing the conduct of clinical studies a plus.
- Benefits:
- A collaborative teamwork environment where learning is constant, and performance is rewarded.
- The opportunity to be part of the team that is revolutionizing the treatment of some of the world's most devastating diseases.
- A generous benefits package for eligible employees that includes medical, dental, vision, life, AD&D, short and long-term disability insurance, 401(k) with employer match, an employee stock purchase plan, paid parental leave, eleven paid company holidays per year, a minimum of fifteen days of accrued vacation per year, which increases with tenure, and paid sick time in compliance with applicable law(s).