Senior Medical Writer, Scientific Communications

Role Overview

• Create high quality scientific communications content to support internal and external data dissemination projects*
• Play a key role in ensuring scientific communication deliverables are completed in a timely manner with stakeholder satisfaction*
• Meet project milestones and escalate challenges as needed to ensure projects remain on track*
• Critically evaluate data and translate information into succinct, scientific summaries*
• Works cross-functionally with the broader clinical, marketing, and creative teams to ensure data dissemination goals and deadlines are met efficiently and effectively
• Work with clinical study management and stats to create timelines for completing data dissemination plans related to clinical studies*
• Prepare regular project status updates to management*
• Prepare and/or edit manuscripts for submission to peer-reviewed journals and publication*
• Prepare abstracts and presentations for submission and presentation at scientific conferences*
• Conduct literature searches for devices and relevant disease states*
• Keep current with literature for relevant disease states and supports maintenance of the clinical literature library*
• Play critical role in supporting and developing scientific communication data dissemination strategy (ex. Journal identification, conference impact, potential sub
• analysis, etc.)
• 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.

Requirements

• Bachelor's degree in science, health, or related field with 5+ years of experience, or equivalent combination of education and experience.
• MS or PhD degree strongly preferred
• 5+ years of experience as a Medical Writer in the biotech/pharmaceutical industry or 5 years of experience in clinical/scientific research, nursing is preferred
• Medical device, pharmaceutical, biotech, or other regulated industry experience desired
• A passion for clarity in written expression
• A style that is equally comfortable working independently and as part of a team
• A body of work that demonstrates outstanding writing skills
• High degree of accuracy and attention to detail
• Proficiency with MS Word, Excel, and PowerPoint
• Excellent organizational skills with ability to prioritize assignments while handling various projects simultaneously
• Excellent communications skills
• 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, 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).