Senior Manager Scientific Communications
Senior Manager Scientific Communications
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Job Description
Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multidimensional expansion to reach more patients through a rich pipeline of differentiated assets led by VYVGART our firstinclass neonatal Fc receptor blocker approved for the treatment of gMG and with the potential to treat patients across dozens of severe autoimmune diseases.
We are building a new kind of biotech company one that maintains its roots as a sciencebased startup and pushes our commitment to innovate across all corners of our business. We strive to inspire and grow our company our partnerships our science and our people because when we do we deliver more for patients.
The key activities that the Senior 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 argenxs SOPs which includes adhering to GPP 2022 and ICMJE best practices.
Roles and 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
Skills and Competencies:
- Understanding of clinical trial design and 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 highquality document
- Independently motivated with good problemsolving skills allowing analysis synthesis and compilation of data from a broad range of disciplines
- Wellorganized with demonstrated ability to prioritize tasks work simultaneously on multiple projects and complete highquality documents according to timelines
- Ability to work in a fastpaced cohesive collaborative teamoriented work environment
Education Experience and Qualifications:
- BS/BA degree in a scientific or healthrelated field required; PharmD PhD or MD preferred
- At least 1 to 5 years of experience in medical/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
#LIHybrid
At argenx all applicants are welcomed in an inclusive environment. They will receive equal consideration for employment without discrimination on the basis of race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other applicable legally protected characteristics. argenx is proud to be an equal opportunity employer.
If you require reasonable accommodation in completing your application interviewing or otherwise participating in the candidate selection process please contact us at . Only inquiries related to an accommodation request will receive a response.
Required Experience:
Senior Manager
Employment Type
Full-Time
