GDO Strategic Support

• Provide an extensive range of leadership and influencing capabilities to achieve the business objectives and goals for both Parexel and clients
• Effectively communicate with internal and external customers as well as third party vendors
• Participate in cross functional meetings and support initiatives to ensure the delivery of milestones and timelines for clinical trials
• Ensure all systems both technical/non-technical are set up for complex projects/programs
• Responsible for the creation and execution of a project timelines plan covering all GDO deliverables; this includes the coordination of dependencies between Data Operation stakeholders (Data Management, Programming, Biostatistics) either within Parexel or at a client
• Work with study teams and Data Standards Associates to ensure enforce the use of data standards as applicable
• Provide technical knowledge and oversight and serve as an escalation point where appropriate.
• Remain informed about developments in relevant regulations and guidelines.

Team Management

• With minimal supervision has the ability to successfully manage a full workload across multiple and varied studies with enthusiasm and prioritize workload with attention to detail
• Ability to work effectively with and motivate virtual teams within different cultural environments
• Ability to negotiate and influence to achieve results project timelines and quality
• Excellent negotiation and diplomacy skills
• Strong customer focus, ability to interact professionally within a client organization
• Ability to identify and address issues proactively
• Efficient time management to meet objectives
• Ability to conduct root cause analysis in business problem solving and process improvements development
• Good understanding of audit/inspection process
• Cultural awareness and ability to think and work globally
• Excellent interpersonal oral and written communication skills
• Capable of adapting and learning quickly
• Managerial courageousness-able to ensure teams stay on track when being challenged. Capable of finding alternative solutions
• Resilience in and ability to adjust to a rapidly changing environment
• Flexibility to change
• Commitment to quality
• Good understanding of and experience in the clinical trial process
• Knowledge of SOPs/guidelines, ICH-GCP and other applicable local and international regulations
• Experience in clinical trial systems and practical knowledge of how these applications fit and work together in Parexel’s standard environment
• Good understanding of the needs and use of data standards in the clinical trial environment
• Efficient project management skills such as communicating with diplomacy and tact, communicating with transparency, learning to be approachable, win new business by running great client facing meetings, Learning to be approachable, and How to build rapport quickly
• Ability to travel locally as well as internationally (as needed) for the position (approximately 20%)
• English proficiency (written and oral English).

Skills:

• With minimal supervision has the ability to successfully manage a full workload across multiple and varied studies with enthusiasm and prioritize workload with attention to detail
• Ability to work effectively with and motivate virtual teams within different cultural environments
• Ability to negotiate and influence to achieve results project timelines and quality
• Excellent negotiation and diplomacy skills
• Strong customer focus, ability to interact professionally within a client organization
• Ability to identify and address issues proactively
• Efficient time management to meet objectives
• Ability to conduct root cause analysis in business problem solving and process improvements development
• Good understanding of audit/inspection process
• Cultural awareness and ability to think and work globally
• Excellent interpersonal oral and written communication skills
• Capable of adapting and learning quickly
• Managerial courageousness-able to ensure teams stay on track when being challenged. Capable of finding alternative solutions
• Resilience in and ability to adjust to a rapidly changing environment
• Flexibility to change
• Commitment to quality
• Good understanding of and experience in the clinical trial process
• Knowledge of SOPs/guidelines, ICH-GCP and other applicable local and international regulations
• Experience in clinical trial systems and practical knowledge of how these applications fit and work together in Parexel’s standard environment
• Good understanding of the needs and use of data standards in the clinical trial environment
• Efficient project management skills such as communicating with diplomacy and tact, communicating with transparency, learning to be approachable, win new business by running great client facing meetings, Learning to be approachable, and How to build rapport quickly
• Ability to travel locally as well as internationally (as needed) for the position (approximately 20%)
• English proficiency (written and oral English).