This role involves collaborating with cross-functional teams, including Medical and Scientific Affairs, Clinical Affairs, and Global Clinical Affairs, to manage and complete studies in compliance with regulations like Good Clinical Practices (GCP), IVDR, and GDPR. The Sr. CPM will guide the planning, execution, and closeout of complex clinical evaluations, from protocol development through study conduct. […]
Additionally, the Sr. CPM will mentor less experienced team members and provide regular communication with internal and external stakeholders to ensure the successful execution of clinical...