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 across projects/programs.

• Drive the implementation of the Data Operations strategy and technology infrastructure for EMEA projects.

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

• Act as the primary point of contact for the Account Lead, functional leaders, clients, and external vendors.

• Ensure that Data Operations deliverables align with timelines, resource allocations, quality, and productivity objectives.

• Manage budgets and resource allocation for designated studies.

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

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

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

• Ensure adherence to data standards while providing technical oversight and escalation support.

• Engage in cross-functional activities, including project kickoff, bid defense, protocol review, and related meetings.

• Organize project tools, plans, Trial Master File, and resource information.

• Supervise technology and data integration team outputs as necessary.

• Guarantee that team members have access to essential tools and documentation.

• Foster collaborative relationships with functional leaders and subject matter experts.

• Offer leadership and direction to project team members.

• Communicate project metric objectives and guide the team towards achieving them.

⛳️ Requirements

• Several years of experience within CRO, Pharma, or Biotech sectors.

• Proven application of project management principles.

• Demonstrated success in leading a project team within a technical/programming, data management, or statistical setting with minimal oversight.

• Strong understanding of cross-functional activities.

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

• Fluent in English.

• Capability to manage a full workload across multiple diverse studies while prioritizing tasks with keen attention to detail.

• Familiarity with SOPs/guidelines, ICH-GCP, and relevant local and international regulations.

• Knowledge of data standards within the clinical trial landscape.

• Proficient project management skills.

• Ability to effectively collaborate with and inspire virtual teams across different cultural environments.

• Strong negotiation and diplomacy skills.

🏝️ Benefits

• Opportunities for professional growth and development.

• Emphasis on work-life balance.

• Flexible working hours.

• A collaborative and inclusive work environment.

• Engagement in groundbreaking projects.