When our values align, there's no limit to what we can achieve.
Role is remote - it can be based in select EMEA locations.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:Global Data Organization (GDO) Strategic SupportProvide an extensive range of leadership and influencing capabilities to achieve the business objectives and goals for both Parexel and clientsEffectively communicate with internal and external customers as well as third party vendorsParticipate in cross functional meetings and support initiatives to ensure the delivery of milestones and timelines for clinical trialsEnsure all systems both technical/non-technical are set up for complex projects/programsResponsible 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 clientWork with study teams and Data Standards Associates to ensure enforce the use of data standards as applicableProvide technical knowledge and oversight and serve as an escalation point where appropriateRemain informed about developments in relevant regulations and guidelinesTeam ManagementProvide an extensive range of leadership and influencing capabilities to achieve the business objectives and goals for both Parexel and clientsEffectively communicate with internal and external customers as well as third party vendorsParticipate in cross functional meetings and support initiatives to ensure the delivery of milestones and timelines for clinical trialsEnsure all systems both technical/non-technical are set up for complex projects/programsResponsible 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 clientWork with study teams and Data Standards Associates to ensure enforce the use of data standards as applicableWith assistance provide input to proposals and attend Bid Defense meetings as requiredAs needed and with guidance, participate in a meeting with Business Development/CDD/PL/PM to understand the scope of the contract and any Master Service Agreement in place for the clientEnsure the operational team reviews the draft protocol from a Data Operations perspectiveAttend project kick off meetings and other project related meetingsReview and collate information required for the project tools, project plan, TMF, resourcing, etc.
in collaboration with the PL/PM.In cooperation with the PL/PM accountable for the deliveries from the technology/data integration team (if applicable)Accountable for ensuring all team members access to tools and documents as requiredEstablish efficient/effective working relationships with other functional leaders and expertsWith assistance provide leadership and direction to the project team membersCommunicate project metric targets to the project team members and guide team towards achieving themIdeal candidate will possess:Several years' experience within CRO/Pharma/BiotechDemonstrated application of project management conceptsProven record of leading a project team in a technical/programming, data management or statistical environment with minimal supervisionProficient understanding of cross-functional activitiesBachelor's degree in a science or industry related disciplineFluent EnglishAbility to successfully manage a full workload across multiple and varied studies with enthusiasm and prioritize workload with attention to detailKnowledge of SOPs/guidelines, ICH-GCP and other applicable local and international regulationsUnderstanding of the needs and use of data standards in the clinical trial environmentProject 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 trustAbility to work effectively with and motivate virtual teams within different cultural environmentsProficient negotiation and diplomacy skillsWhy 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.