工作职责
● Scientific Writing:
● Develop, write, and edit high-quality scientific documents, including study protocols, clinical study reports (CSRs), manuscripts, and presentations.
● Ensure all documents are scientifically accurate, clear, and compliant with regulatory requirements and company standards.
● Publication Process Management:
● Oversee the internal publication review process, coordinating feedback from various stakeholders to ensure timely and effective document revisions.
● Act as the main point of contact for the Bayer China publication team, facilitating communication and collaboration with global publication teams.
● Collaboration and Liaison:
● Work closely with cross-functional teams, including clinical research, regulatory affairs, and medical affairs, to gather relevant data and insights for scientific writing.
● Collaborate with external authors, researchers, and subject matter experts to ensure comprehensive and accurate representation of scientific findings.
● Quality Assurance:
● Implement and maintain quality control processes for all written materials to ensure consistency and adherence to best practices in scientific writing.
● Stay updated on industry trends and guidelines related to scientific writing and publication standards.
● Publication Strategy Development:
● Develop and implement a comprehensive publication plan that aligns with the company’s objectives and complies with regulatory requirements.
● Identify key messages and target audiences for publications to maximize impact.
● Stakeholder Engagement:
● Engage with key stakeholders, including regulatory affairs and marketing teams, to ensure alignment on publication strategies and messaging.
● Facilitate communication between authors and stakeholders to streamline the publication process.
● Monitoring and Performance Tracking:
● Monitor the impact of publications through metrics such as citations and journal impact factors, and adjust strategies as needed.
● Stay informed about trends in publication practices and regulatory changes that may impact publication strategies.
● Training and Mentorship:
● Provide guidance and training to junior writers and team members on scientific writing best practices and publication processes.
● Timelines and Project Management:
● Manage timelines for document preparation and publication activities, ensuring timely delivery to meet project deadlines.
任职要求
● Doctoral degree (PhD, MD, or PharmD) in Life Sciences, Medicine, Pharmacy, Public Health, or a related field is preferred.
● Proven experience (7+ years) in medical or scientific writing within the pharmaceutical or biotechnology industry, with a strong focus on the publication process.
● Demonstrated expertise in writing and preparing high-quality scientific documents in Chinese and English, including:
● Clinical Study Reports (CSRs)
● Study Protocols
● Manuscripts for peer-reviewed journals
● Abstracts and presentations for scientific conferences
● A strong publication record with experience in navigating the manuscript submission process, including familiarity with journal requirements, peer review processes, and responding to reviewer comments.
● Exceptional writing and editing skills with a strong attention to detail, ensuring clarity and accuracy in scientific communication.
● Ability to interpret complex scientific data and convey it in a clear, concise, and engaging manner for diverse audiences.
● Strong organizational and project management skills, with the ability to manage multiple writing projects simultaneously and meet tight deadlines.
● Excellent interpersonal and communication skills, with the ability to collaborate effectively with cross-functional teams and external partners.
● Proficiency in referencing and citation management tools, as well as familiarity with relevant guidelines for scientific writing (e.g., CONSORT, ICMJE).