Job Summary
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.
Main Responsibilities
* Manage complex clinical evaluations, prepare and review essential study documents, and oversee relationships with Contract Research Organizations (CROs), vendors, and clinical sites.
* Represent Medical and Scientific Affairs in interactions with investigators, site staff, Ethics Committees, Health Authorities, and Key Opinion Leaders to ensure the success of clinical studies.
* Mentor less experienced team members and provide regular communication with internal and external stakeholders.
About You
An advanced degree in a relevant scientific discipline or a master's degree in Biological Sciences or Biomedical engineering focused on Biotechnology is required. A minimum of 6 years of relevant industry experience in product development or a combination of equivalent education and experience is also required.
Experience in clinical laboratory work, previous experience with BD Biosciences systems and reagents, and knowledge of MS Office, strong skills with MS Excel, EndNote, Pubmed, Medline, and/or database development are preferred qualifications.