Remote Senior Medical Writer - Immunology
Posted 2025-08-15
Remote, USA
Full Time
Immediate Start
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
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