Senior Scientific Communications Manager

Full Time On-Site/Hybrid Marketing Communications Manager Apply for this Job The Senior Scientific Communications Manager will report directly to the Head, Publications. The key activities that the Scientific Communications Manager will facilitate, and support include abstracts, posters, and oral presentations at scientific congresses, submission of manuscripts to scientific journals. The individual will be responsible for adhering to and supporting all of argenx's SOPs, which includes adhering to GPP 2022 and ICMJE best practices.

Key Accountabilities/Responsibilities:

• Manage the overall development and approval process for assigned documents within timelines, including documentation generation, initiation of review process, discussions on proposed revisions, and document completion in collaboration with other team members
• Coordinate internal stakeholder and author interactions, develop project timelines, maintain compliance with publication industry and company standards and ensure timely achievement of project milestones
• Supervise/monitor communications vendors to optimize timely development of materials
• Ensure timely communication and follow up with all key stakeholders
• Provide updates of scientific publication activities on a regular basis and/or as directed which may include provision of updates in PowerPoint, word, or other formats
• Ensure all publication activities are appropriately archived

Desired Skills and Experience:

• Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting requirements
• Ability to work collaboratively and coordinate the efforts of team members to resolve comments, and produce a final high-quality document
• Independently motivated with good problem-solving skills allowing analysis, synthesis and compilation of data from a broad range of disciplines
• Well-organized with demonstrated ability to prioritize tasks, work simultaneously on multiple projects, and complete high-quality documents according to timelines
• Ability to work in a fast-paced, cohesive, collaborative team-oriented work environment

Education and Qualifications:

• BS/BA degree in a scientific or health-related field required; PharmD, PhD or MD preferred
• At least 1 to 5 years of experience in medical/regulatory/publication writing in the pharmaceutical, biotech, device, medical communications, or CRO industries
• Demonstrated ability to produce clear, concise, and effective written and verbal communications describing scientific and clinical data in English
• Demonstrated ability to write clear, concise, and effective publications, including the ability to turn data into visuals that convey the key messages and to communicate complex information effectively and accurately