With operations in 35+ nations and 20,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza.
Our therapies are also used in cardiac surgery, organ transplantation and burn treatment. CSL is the parent company of CSL Behring and Seqirus.
CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions.
CSL Behring operates CSL Plasma , one of the world's largest collectors of human plasma, which is used to create CSL’s therapies.
Seqirus is the second largest influenza vaccine company in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally.
We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team! Responsibilities Qualifications Together into the Future.
depth understanding of the therapy area and its research advancements and communicating both the depth of science behind CSL’s medicines and develop scientific partnerships to facilitate the quality use of our medicines.
Main Responsibilities and Accountabilities : Work collaboratively and proactively with the Cross-Functional Team to develop strategic medical, scientific and relationship management plans that align with business objectives Provide medical input into key cross-
functional groups (including but not limited to) : Regulatory; Clinical Safety; Health Outcomes; Clinical R&D, Manufacturing and Quality for successful development and life cycle management of products Key-
member of the new product introduction process (pre-launch, launch). Responsible for leading medical activities required for this process.
Provide a high-quality single point of contact for scientific interaction between external experts / HCP’s and CSL Behring Interact responsibly and within governance and compliance guidelines (and / or relevant Country Codes) with targeted health care professionals, professional associations and other key stakeholders Assist with publication planning and presentations of data at medical & scientific meetings.
Appropriately understand the clinical gaps that would facilitate the development of new therapeutic agents / indications Ensure engagement plans are initiated and actively managed for identified External Experts (EE) Facilitate speaker management and involvement locally and internationally Ensure appropriate EE development through participation in clinical trials Develop and maintain extensive knowledge of the designated therapeutic area(s), pipeline and the competitive landscape Qualifications : University degree : Physician, Pharmacist, Master of Science in Biomedical Sciences, PhD in a relevant scientific field would be highly desirable At least 2 years of appropriate experience with demonstrated relevant competencies required to qualify for this role Ability to apply and leverage scientific and medical knowledge is essential Prior experience providing MSL level support to products in specific therapeutic areas Strong negotiation, influencing and leadership skills Excellent presentation, interpersonal and communication skills Demonstrated ability to manage relationships with external experts Demonstrated business planning ability and strong organizational skills Demonstrated innovative thinking Demonstrated working knowledge of regulations governing information provision / interactions with customers within the pharmaceutical industry.
Strong medical governance capabilities. Strong strategic thinking capabilities Ability to work independently & be self-motivating #Behring Capabilities Worker Type : Employee Worker Sub Type : Regular