The base salary range for this position will be $135,000 - $150,000. What you will be doing: Planning and implementation of cross-functional projects within the trials. Facilitate the definition of project scope, goals and deliverables Define project tasks and resource requirements. Develop full-scale cross-functional project plans. Assemble and coordinate project staff Plan and schedule project timelines Develop and Manage Risk Mitigation Strategies for projects Track project deliverables using appropriate tools Constantly monitor and report on progress of the project to all stakeholders Implement and manage project changes and interventions to achieve project outputs Project evaluations and assessment of results Manage project study budgets and invoicing procedures according to study contract What you will bring to the organization: Bachelor's Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or related field Minimum 6 months-2 years of experience in a CRO/Sponsor or clinical project management capacity Knowledge of ICH/GCP/FDA regulations and guidelines for medical devices and/or pharmaceutical/biologic agents A forward thinking and positive attitude Self-motivation