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
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