Job DescriptionThis role based in Mexico will be key to further develop the country capabilities in clinical research. Under the oversight of the country CRD, the person will be responsible for the end-to-end performance of clinical trials in one or several TA, from feasibility to close out in one or several countries.The role should be responsible for 30 to 50 clinical trials and will ensure excellent study performance with strict adherence to local regulations, SOPs, and ICH GCP.The role is responsible for oversight of all the employees working in the TA, with line management for CRMs and functional oversight of other roles in his studies. As line manager, the role is critical to develop key talents in the organization to ensure a pool of successors in critical roles.The role will work at the country level with other local stakeholders like GMA, GHH, PV, and regulatory to ensure alignment and development of the country capabilities and can represent the CRD of the cluster in local management if required. CRD can delegate certain key tasks as needed.Responsibilities include, but are not limited to:Will lead 1 or several TA of the growing portfolio in the countryAccountable for the successful execution, enrollment, and quality of their clinical trial portfolioAccountable to ensure timelines and key milestones are metAccountable for performance metricsAccountable to develop operational strategies and quality plans for the conduct of all programs and studies in the TA portfolioCollaborates with other TA directors, local and regional stakeholders in GCTO in order to develop and build territory of principal investigators and sitesEnsures oversight and line management of Clinical Research Manager (CRM) team within TALeads team independently with supervision from CRD to high performanceAccountable for CRM performance reviews, including addressing low performance situations, and taking appropriate actionsEnsures key talent development and retentionCollaborates and works closely with other stakeholders in the TA in GCTO & GCD regional and headquarter teams, quality, finance, IT, and HRCollaborates externally with investigators, regulators, and vendorsMember of the GCTO country leadership teamSupports strategic initiatives across Global Clinical Development GCD and GCTOSupports local strategy development consistent with long-term corporate needs in conjunction with CRDTogether with direct reports, contributes significantly to effective conduct of clinical studies and to develop the pipeline, while maintaining regulatory requirements and complianceThis position impacts directly the country's ability to reach business targets and objectives and ensures that productive collaboration with internal and external business partners are built#J-18808-Ljbffr