Sr Clinical Trial Manager - Global Studies

Sr Clinical Trial Manager - Global StudiesThe Sr Clinical Project Manager provides management of a clinical trial(s) in a global level. Services/deliverables include operational oversight of assigned project(s) at the global level for end-to-end project management from start-up through to closeout activities.Tasks & Responsibilities:Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).Accountable for meeting projects' recruitment targets and ensuring appropriate recruitment strategies are in place.Contribute to the development of the project risk mitigation plan and manage clinical risks throughout the project's lifecycle.Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.Essentials Requirements:Bachelor's Degree Health care or other scientific discipline ReqRequires 8 years clinical research/monitoring experience or equivalent combination of education, training and experience.Minimum 3 years of regional/global trial management experience in the pharmaceutical industry or CRO.Requires in-depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Where you'll workYou'll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you'll stay connected while enjoying the autonomy and balance that comes with a fully remote role.