Remote Logistics Strategist: Optimize Shipments & Partners

Placements24; East London; Remote; ZAR 1,000,000 - 1,400,000; Full time

Job summary

Parexel is seeking a Biometrics Delivery Lead to oversee data operations strategy and technology setup for EMEA projects. The role leads database programming, data management and statistical services, coordinating across global teams and clients to meet timelines and budgets.

The ideal candidate has CRO/Pharma/Biotech experience, strong project management and leadership skills, and fluency in English. This is a senior, cross-functional role requiring regulatory knowledge and effective

Qualifications

• Several years' CRO/Pharma/Biotech experience.
• Demonstrated project management concepts application.
• Proven record of leading a project team in technical/programming, data management or statistics.
• Proficient understanding of cross-functional activities.
• Bachelor's degree in a science or industry related discipline.
• Fluent English.
• Ability to manage a full workload across multiple studies with attention to detail.
• Knowledge of SOPs/guidelines, ICH-GCP and relevant regulations.
• Understanding of data standards in the clinical trial environment.
• Project management skills: presentation, public speaking, communication.

Responsibilities

• Provide leadership and influencing capabilities to achieve objectives for Parexel and clients.
• Communicate effectively with internal/external customers and third-party vendors.
• Participate in cross-functional meetings to ensure milestones and timelines for clinical trials.
• Ensure all systems, technical and non-technical, are set up for complex projects/programs.
• Create and execute project timelines covering all GDO deliverables; coordinate dependencies across stakeholders.
• Work with study teams and Data Standards Associates to enforce data standards as applicable.
• Provide technical knowledge and serve as escalation point where appropriate.
• Stay informed about developments in relevant regulations and guidelines.

Skills

CRO/Pharma/Biotech experience

Project management

Leadership of project team

Cross-functional collaboration

Fluent English

workload management

Data standards understanding

Negotiation & diplomacy

Public speaking / presentation

Education

Bachelor's degree in science or related field

Job description

**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
• 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