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CSL Behring is a global biotechnology leader, guided by a promise to save and improve lives. Millions of people around the world are living with rare and serious medical conditions. CSL Behring is committed to delivering medicines that improve their lives.
With operations in 35+ nations and ~ 30,000 employees worldwide, CSL is inspired 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, CSL Plasma, CSL Seqirus and CSL Vifor. 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.
Could you be our next Project Manager of Adaptive Trial Clinical Trial of Technologies? The job is located in our King of Prussia PA office. This is a hybrid position. You will report to the Associate Director of eClinical Operations.
You will be the primary contact for clinical trial technology used in project(s), working with the study teams and vendor project leadership to achieve study goals.
Responsible for overall management and execution of the technology for the project(s) and coordination of all related activities on a study team.
You will support vendor compliance through the CSL Audit Process to ensure that the vendor has the appropriate Quality Management, planning, and resourcing in place to support CSL Projects.
Interpret the study protocols to assess all possible requirements for technology used in the project(s), in addition to those specified during the relevant study team meetings.
You will support development of project related documentation for the technology used during the course of the Project Lifecycle.
Guide the study team in the development of the specifications and validation plan for the clinical trial technology-paying specific attention to all the project deliverables.
Ensure that the vendor(s) maintains high-quality service and delivery of data and technical project(s) outputs for the customer.
Educated to BA or BS Degree level
Experience in a Project Management role OR equivalent, related to the pharmaceutical or clinical research industry
3+ years experience at another sponsor or vendor in a role supporting implementation of clinical trial technologies (eCOA, eConsent, biosensors)
Experience the clinical research environment and GCP principles
BENEFITS
Medical, Dental Vision
401K
Paid time Off
#LI-HYBRID
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.
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.
As a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.
