Responsibilities: Under general direction, serves as medical expert and contributes to strategic product plan for the region/country Implements strategy for scientific interactions with the medical community including key opinion leaders and patient advocacy groups Supports medical affairs operations on logistical planning and implementation of projects, including supporting and delegating activities to ensure prompt turnaround and project success Coordinates the review of Investigator Initiated Research (IIR) study proposals Serves as medical consultant and supports commercial, marketing and sales organizations Qualifications: Degree in nursing, pharmacy or advanced degree in science/medicine (MD, PhD, PharmD) preferred 5+ years' relevant pharmaceutical/ biopharmaceutical industry experience General clinical trial experience Knowledge of therapeutic specialty area Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.
Our Benefits
CSL Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives. Learn more about some of the benefits you can participate in when you join CSL Seqirus.
About CSL Seqirus
CSL Seqirus is part of CSL Limited (ASX: CSL). As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. Learn more about CSL Seqirus.
We want Seqirus to reflect the world around us
As a global organisation with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL Seqirus.
Do work that matters at CSL Seqirus!
Watch our ‘On the Front Line’ video to learn more about CSL Seqirus