Biometrics Delivery Lead
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Job Description
Biometrics Delivery Lead overseeing clinical-trial data operations, technology, and delivery for Parexel’s EMEA projects. Leading cross-functional teams, budgets, timelines, and client-facing execution.
Responsibilities:
- Provide overall leadership and management for database programming, data integration, data management, statistical services and medical writing on projects/programs
- Lead execution of the Data Operations strategy and technology setup for EMEA projects
- Oversee Global Data Operations team members and activities across geographies
- Liaise with account leads, functional leaders, Parexel teams, clients and third-party vendors
- Ensure Data Operations deliverables meet timelines, resourcing, quality and productivity requirements
- Manage budgets and resourcing for assigned studies
- Set up technical and non-technical systems for complex projects/programs
- Create and execute project timeline plans covering Global Data Organization deliverables
- Coordinate dependencies among Data Management, Programming and Biostatistics stakeholders
- Ensure use of applicable data standards
- Provide technical oversight and serve as an escalation point
- Participate in cross-functional, kickoff and project-related meetings
- Review protocols from a Data Operations perspective
- Coordinate project tools, project plans, TMF and resourcing information
- Oversee technology/data integration team deliveries where applicable
- Ensure team access to required tools and documents
- Provide leadership and direction to project team members
- Communicate project metric targets and guide teams toward achieving them
Requirements:
- Several years’ experience within CRO/Pharma/Biotech
- Demonstrated application of project management concepts
- Proven record of leading a project team in a technical/programming, data management or statistical environment with minimal supervision
- Proficient understanding of cross-functional activities
- Bachelor’s degree in a science or industry related discipline
- Fluent English
- Ability to successfully manage a full workload across multiple and varied studies with enthusiasm and prioritize workload with attention to detail
- Knowledge of SOPs/guidelines, ICH-GCP and other applicable local and international regulations
- Understanding of the needs and use of data standards in the clinical trial environment
- Project management skills
- Ability to work effectively with and motivate virtual teams within different cultural environments
- Proficient negotiation and diplomacy skills
Benefits:
- Professional growth and development opportunities
- Work-life balance
- Flexible working hours
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