Remote Senior Medical Writer - Immunology

About the position Responsibilities • Serve as medical writing lead on assigned projects, collaborating with cross-functional teams on project strategies. • Coordinate the review, approval, and production of writing projects, including arranging review meetings and ensuring documentation is obtained. • Convert relevant data and information into formats that meet project requirements, explaining data in a manner consistent with target audience needs. • Communicate deliverables, writing processes, and timelines effectively to team members, holding them accountable for project dates and quality levels. • Negotiate with functional areas on project outcomes and deliverables, identifying and proposing solutions to issues arising during the writing process. • Interpret and explain data from various sources, ensuring results are consistent with protocols and challenging conclusions when necessary. • Perform literature searches for drafting document content and make recommendations for application to writing projects. • Work with journals and congresses throughout the writing process, addressing questions and drafting responses as necessary. • Stay knowledgeable of US and international regulations related to writing projects, continually training to comply with industry requirements. • Act as a representative on project teams, mentoring junior writers and implementing process improvements. Requirements • Bachelor of Science or Bachelor's degree in English or communications with relevant science experience; advanced degree preferred. • 3 years of relevant industry experience in medical writing or related areas such as quality, regulatory, publications, clinical research, or product support/R&D. • Knowledge of US and international regulations associated with writing projects. • Excellent written and oral communication skills, with experience in collaborative, cross-functional teams and project management. • Ability to assimilate and interpret scientific content and translate information for appropriate audiences. • Superior attention to detail and ability to correct errors in spelling, punctuation, grammar, and clarity. Nice-to-haves • American Medical Writing Association (AMWA) certification or similar, with a specialty in Editing/Writing or Pharmaceutical. • 3 years of experience in experimental design and clinical/preclinical data interpretation. • Experience working with templates and relevant systems. Benefits • Paid time off (vacation, holidays, sick) • Medical, dental, and vision insurance • 401(k) plan • Short-term incentive programs • Long-term incentive programs Apply tot his job Apply To this Job