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Clinical Project Managers are an integral part of clinical trial delivery, working alongside clinical teams to improve patients' lives by bringing new drugs to the market faster.
The CPM is a member of the core project team responsible for clinical delivery of clinical studies to meet contractual requirements in accordance with Standard Operating Procedures (SOPs), policies and practices.
You will: 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.Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.What do you need to have? Advanced degree or equivalent education/degree in life science/healthcare recommended.7 years clinical research/monitoring experience; or equivalent combination of education, training and experience.At least 2-3 years leading clinical research studies (regional and/or globally speaking).
Involvement in cross-functional, multicultural and international clinical trials; demonstrated capabilities in supporting operational aspects of clinical trial related activities.Fluent English (oral and written).
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