The position is responsible for supporting the development and execution of harmonized global publication plans across selected mature legacy in-line therapeutic areas at CSL Behring. This includes author interactions, writing, and vendor management in conjunction with Good Publication Practices, internal guidance documents, and requires effective cross-functional alignment during the planning process and communication during all portions of execution of the plans.

Responsibilities:

•Partners with Medical TA leads and Pubs Director to develop strategic publication plans for select mature legacy in line products•Responsible for execution of assigned publications according to timelines of the publication plans •Responsible for vendor management relating to assigned publications•In collaboration with Pubs Director, engage internal and external authors and other key stakeholders in the development of publication plans and strategy at the individual dataset, study, and/or compound level.•With guidance of Pubs Director, assist executing on completion of abstracts, posters/oral presentations and manuscript in compliance with standard operating procedures/industry standards. •Follow international guidelines including but not limited to International Committee of Medical Journal Editors (ICJME), Good Publication Practices (GPP), CONSORT Guidelines, American Medical Association (AMA) Manual of Style, and Council of Biology Editors.•Participate in the development and maintenance of document templates, style guides, electronic document management and publication review and approval system.•Ensure utilization of the PubsHub globally for all publication-related activities.•In collaboration with Pubs Director, provide oversight of completed, ongoing and future publications and manage a publication tracker for assigned products•Ensure appropriate copyright is obtained for all MA related assets

Qualifications:

•Degree in nursing, pharmacy or advanced degree in science/medicine (MD, PhD, Pharm D, MS) preferred with 5+ years of relevant pharmaceutical/biopharmaceutical industry or relevant experience •Experience working in matrixed teams in a global organization•Experience in biomedical research, scientific analysis and writing•Experience in vendor management•Project management is a plus

Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.

Our Benefits

CSL employees that work at least 30 hours per week are eligible for benefits effective day 1. We are committed to the wellbeing of our employees and their loved ones. CSL offers resources and benefits, from health care to financial protection, so you can focus on doing work that matters. Our benefits are designed to support the needs of our employees at every stage of their life. Whether you are considering starting a family, need help paying for emergency back up care or summer camp, looking for mental health resources, planning for your financial future, or supporting your favorite charity with a matching contribution, CSL has many benefits to help achieve your goals.

Please take the time to review our benefits site to see what’s available to you as a CSL employee.

About CSL Behring

CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring.

We want CSL to reflect the world around us

As a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.

Do work that matters at CSL Behring!