Carrie Guglielmo Email & Phone Number

Basel, Baselstadt, Ch

Basel, Baselstadt, Ch

Basel, Baselstadt, Ch

Served as one of six Global Resource Managers. Responsible for the full performance management life cycle and strategic resourcing for Clinical Managers in Global Clinical Trial Management. Managed up to thirty globally based Clinical Managers and Planners of Clinical Operations in US, Switzerland and India. Established new reporting structure and supported teams through role transformation. Responsible for the strategic management of resource allocation to support the global clinical programs, including alignment of prioritization of projects. Ability to identify inefficiencies with daily tasks and provide guidance on improvement that ultimately lead to greater productivity.

Basel, Baselstadt, Ch

Switzerland 🇨🇭 , Ch

Managed twelve in-house Clinical Operations Associates, Clinical Trial Associates, and one administrative associate and served as one of four Functional Managers for US Affiliate. Established new reporting structure in organization. Collaborated with colleagues in South San Francisco and Canada to align management directives, training and processes. Communicated corporate messages, performance feedback and key decisions to stakeholders and direct reports while ensuring productivity and engagement. Identified issues and created solutions for obstacles hindering successful achievement of critical goals. Demonstrated resiliency and professionalism during extreme ambiguity and fostered this same attribute with direct reports and colleagues.

Switzerland 🇨🇭 , Ch

Lead and managed team of Field Clinical Trial Monitors, Clinical Operations Associates, and Clinical Trial Associates in first Alzheimer’s study. Identified Investigators and Scientific Thought Leaders for new therapeutic area•Identified and managed critical issues by developing and updating plans for risk management and contingency.•Performed forecasting and management of $1.2 million budget.•Created and implemented project and site level project recruitment plans that provided accuracy and met company projections.•Collaborated with multiple vendors assigned to support training needs of both internal and external staff. Ensured country commitments were achieved. •Created study tools to assist with site recruitment and patient participation

Switzerland 🇨🇭 , Ch

Supported daily activities across all phases of study management including feasibility, site selection, start-up, conduct, and close-down.•Acted as liaison for all daily interactions with key stakeholders, including monitors, study management, data management, and clinical science.•Reviewed, collected, submitted and reconciled regulatory documents•Performed ongoing status review of monitor, site, and patient issues, escalating critical issues, while suggesting risk mitigation strategies.