Responsibilities:

Assists in the preparation of new drug application safety updates, investigational new drug safety reports, investigator communications, product labeling/package inserts and other reports as necessary.May work with data management in the ongoing development and maintenance of databases.Responsible for supporting the GCSP with safety data analyses data retrieval from the GCSP safety database. Provide PL/SQL to analyses the safety database and/ or retrieve data as needed. In addition, other software tools will be used as appropriate. Contribute to the establishment of standard programs, standard procedures and work practices to ensure quality control and audit trails for analyses appropriate for regulatory submissions and publication.This role has global responsibilities with potential for matrix management , participation in global teams, and requires skills in leadership without formal authority.

Qualifications:

Requires medical background with 3+ years' pharmaceutical experience.Previous experience and/or knowledge of Pharmacovigilance.Good understanding of medical terminology.

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

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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.

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

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