Biometrics Delivery Lead

This is a fully remote position, open to applicants in South Africa.

📋 Description

• Provide comprehensive leadership and management for database programming, data integration, data management, statistical services, and medical writing on projects/programs.

• Spearhead the execution of the Data Operations strategy and technology configuration for EMEA projects.

• Supervise Global Data Operations team members and activities across various regions.

• Collaborate with account leads, functional leaders, Parexel teams, clients, and third-party vendors.

• Ensure that Data Operations deliverables align with timelines, resourcing, quality, and productivity standards.

• Manage budgets and resource allocations for assigned studies.

• Establish both technical and non-technical systems for complex projects/programs.

• Develop and implement project timelines that encompass Global Data Organization deliverables.

• Coordinate dependencies among stakeholders in Data Management, Programming, and Biostatistics.

• Ensure compliance with applicable data standards.

• Provide technical oversight and act as an escalation point.

• Participate in cross-functional, kickoff, and project-related meetings.

• Review protocols from the standpoint of Data Operations.

• Organize project tools, project plans, TMF, and resource information.

• Oversee deliveries from the technology/data integration team where applicable.

• Ensure team members have access to necessary tools and documents.

• Offer leadership and guidance to project team members.

• Communicate project metric targets and assist teams in achieving them.

⛳️ Requirements

• Several years of experience in CRO/Pharma/Biotech.

• Demonstrated application of project management principles.

• Proven track record of leading a project team in a technical/programming, data management, or statistical environment with minimal supervision.

• Strong understanding of cross-functional activities.

• Bachelor’s degree in a science or related industry discipline.

• Fluent in English.

• Ability to effectively manage a full workload across multiple and diverse studies with enthusiasm, while prioritizing tasks with attention to detail.

• Knowledge of SOPs/guidelines, ICH-GCP, and other applicable local and international regulations.

• Understanding of the requirements and application of data standards in the clinical trial context.

• Strong project management skills.

• Ability to work effectively and motivate virtual teams within diverse cultural settings.

• Proficient negotiation and diplomacy skills.

🏝️ Benefits

• Opportunities for professional growth and development.

• Work-life balance.

• Flexible working hours.