Biometrics Delivery Lead

The Senior Biometrics Delivery Lead, reporting into the Global Biometrics Account Lead (AL) or Global Biometrics Group Lead (GBGL), has overall accountability for the execution of the Data Operations strategy and the Data Operations technology set up for the project. The Senior DL provides overall leadership/management for database programming, data integration, data management, statistical and medical writing services 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 Senior DL will be responsible for managing budgets and resourcing for assigned studies. The Senior DL may take on some AL responsibilities for projects involving a small number of services, where no account lead is assigned. Senior DLs may mentor junior staff and Functional Leads for specific projects. Main responsibilities include GDO Strategic Support and Team Management. 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
• Provide technical knowledge and oversight and serve as an escalation point where appropriate
• Remain informed about developments in relevant regulations and guidelines
• With assistance provide input to proposals and attend Bid Defense meetings as required
• Ensure the operational team reviews the draft protocol from a Data Operations perspective
• Review and collate information required for the project tools, project plan, TMF, resourcing, etc. in collaboration with the PL/PM.
• Accountable for ensuring all team members access to tools and documents as required
• Ensure information entered in internal management systems is accurate and updated on a regular basis
• Establish efficient/effective working relationships with other functional leaders and experts
• With assistance provide leadership and direction to the project team members
• Communicate project metric targets to the project team members and guide team towards achieving them
  
  Several years' experience within CRO/Pharma/Biotech
• Proven record of leading a project team in a technical/programming, data management or statistical environment with minimal supervision
• Bachelor's degree in a science or industry related discipline
• 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
• Project management skills such as improving presentation skills, public speaking foundations, proficiency in delivering impactful presentations to various audiences, speaking confidently and effectively
• Ability to adapt communication style to achieve optimal results in various professional contexts to enhance conversational outcomes
• Proficient negotiation and diplomacy skills
  
  When you join us, you're joining a team that sees everything they do as an opportunity to transform the world for patients everywhere. When our employees bring their many perspectives together to tackle a new challenge, there's no limit to what they can accomplish. Through it all, at the center of all we do, is a patient whose life could change - forever. And together, we'll do it With Heart ., Parexel is among the world's largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help lifesaving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory, and therapeutic expertise, our team of more than 21,000 global professionals works in partnership with biopharmaceutical leaders, emerging innovators, and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere.
  
  Why join us:
Opportunity to work on innovative projects at the forefront of the industry Collaborative and inclusive work environment that values your expertise Professional advancement and development opportunities Work life balance and flexible working hours