Clinical Services and Capabilities Associate Our client, a global pharma company, are currently recruiting for a Clinical Services and Capabilities Associate to join their team on a permanent basis.
As Clinical Services and Capabilities Associate you will be responsible for delivering the implementation of clinical capabilities including to mobile health care, telemedicine, virtual trial orchestration, recruitment & retention, new site models, central services and/or digital devices.
This role will also be responsible for vendor management to support the capabilities team.
Responsibilities Understand business strategies, processes, and technology as it relates to clinical services and capabilities Serve as domain expert to ensure data, process and/or technology capabilities are optimized across the group Maintain strategic alignment for clinical services across functional and therapeutic areas Implement clinical services and capabilities strategy and plan Continuously maintain a state of inspection readiness.
Participate and perform duties required for internal and external inspections as well as supporting institutions/investigators and alternative site locations in inspection readiness initiatives Drive continuous improvement, shared learning, and process expertise between teams Develop critical success factors for pilots/projects and monitor progress to ensure clear criteria exists to enable decision making Identify, monitor, and communicate global customer (internal and external) needs/requirements related to process and/or technology performance and improvements Lead organizational change, communication planning and training initiatives Provide guidance and consulting into forecasting and managing expenses Identify project implementation risks and raise issues appropriately Lead progress reporting activities and metrics Foster inclusion, innovation, and promote diversity Partner closely within team to effectively plan, forecast, and manage the portfolio and project work Collaborate with vendors to improve customer experience and monitor performance Requirements Bachelor's degree and 1-2 years of experience in project management, clinical drug development or a health care related field Demonstrated ability to implement strategies to improve processes and capabilities Strong networking, interpersonal and relationship skills with demonstrated ability to work in teams, across organizational boundaries and achieve results through others Knowledge of emerging health care related services and capabilities for clinical research Knowledge of country regulatory guidelines/requirements for clinical research conduct Flexibility to adjust quickly to changing business priorities Good interpersonal and leadership skills Excellent oral and written communication skills Strong business insight Flexibility (start / finish time daily) Open to potential evening shift work (Mon-Fri only) For more information contact Sinéad Cullen at siné****** or