Remote Logistics Strategist: Optimize Shipments & Partners

Picture Yourself At Parexel:

The Biometrics Delivery Lead (DL), reporting into the Global Biometrics Account Lead (AL) has overall accountability for the execution of the Data Operations strategy and the Data Operations technology set up for the EMEA project. The DL provides overall leadership/management for database programming, data integration, data management, statistical services and medical writing on a project/program. General areas of responsibility include oversight of the Global Data Operations team members and their activities across all geographies, liaising with the AL, other functional leaders (both in GDO and across Parexel), and the client as a single point of contact to ensure that the Data Operations deliverables regarding timelines, resourcing, quality, and productivity are being met. The DL will be responsible for managing budgets and resourcing for assigned studies.

The DL may take on some AL responsibilities for projects involving a small number of services, where no account lead is assigned.

What You'll Do At Parexel:

• 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

Ideal candidate will possess:

• 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 such as improving presentation skills, public speaking foundations, speaking confidently and effectively, boosting your confidence, public speaking and performance, delivery tips for speaking in public, Centered communication: get better results from your conversations, critical thinking and building trust
• Ability to work effectively with and motivate virtual teams within different cultural environments
• Proficient negotiation and diplomacy skills

Why join us:

Be part of groundbreaking projects that are pushing the boundaries of the industry. Experience a collaborative and inclusive work environment that highly appreciates your expertise. Unlock your full potential with professional growth and development opportunities. Enjoy