The Senior Clinical Project Manager (Sr. CPM) will lead and oversee clinical performance evaluation studies for BD devices in Europe, focusing on the procurement of human bio-specimens for analytical and clinical studies.
Key Responsibilities:
* Managing complex clinical evaluations
* Preparing and reviewing essential study documents
* Overseeing relationships with Contract Research Organizations (CROs), vendors, and clinical sites
The Sr. CPM will manage budgets, timelines, and resources, ensuring studies are executed on schedule and within budget. They will also be responsible for identifying suitable clinical sites, managing training materials, ensuring the study trial master file is complete, and addressing risks.
Mentoring less experienced team members and providing regular communication with internal and external stakeholders to ensure the successful execution of clinical trials is also a key responsibility of the Sr. CPM.
About You:
* Education: Advanced degree in relevant scientific discipline (PhD, PhamD, MD) or master's degree (Biological Sciences or Biomedical engineering focused on Biotechnology)
* Minimum of 6 years of relevant industry experience in product development or a combination of equivalent education and experience, preferable with in-vitro diagnostics
Experience in clinical laboratory work, previous experience with BD Biosciences systems and reagents, and experience using flow cytometric analysis software are highly desirable qualifications for this role.