Senior / Principal Statistician X1
Job Details
- Position Title: Senior / Principal Statistician
- Location: Bloemfontein, South Africa
- Company: Metronomia Clinical Research (South Africa) (Pty) Ltd
- Industry: Clinical Research / CRO
- Team: Biometrics / Biostatistics
- Employment Type: Full-time
- Work Model: Flexible / family-friendly working concepts
- Experience Level: Senior (5–10 years)
- Reports to: Head of Biometrics / Biostatistics Lead (typical)
- Contact:
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Lachaé Leo – lleo@metronomia.net
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Christoph Hortian – chortian@metronomia.net
Job Overview
As a Senior / Principal Statistician, you will lead and manage biostatistical services for clinical trials, acting as the primary statistical expert and client liaison. You will oversee project delivery, manage budgets, supervise project teams, and ensure compliance with regulatory and CDISC standards. This role requires strong technical expertise, leadership skills, and the ability to communicate effectively with clients and internal stakeholders.
Key Responsibilities
Project & Team Leadership
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Lead biostatistical project teams and provide technical supervision across clinical trial phases.
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Manage the statistical activities for clinical trials from planning to reporting.
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Serve as the primary point of contact for clients regarding statistical matters.
Project Management & Budgeting
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Manage project budgets, including cost proposal preparation and performance reporting.
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Ensure projects are delivered on time, within budget, and with high quality.
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Attend bid defense meetings and present statistical service offerings, including programming and operational bids.
Client & Regulatory Interaction
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Represent Biometrics in governance meetings, regulatory inspections, and client audits.
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Maintain strong relationships with sponsors and clients, ensuring clear communication and client satisfaction.
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Ensure all biostatistical deliverables meet regulatory and client expectations.
Your Profile
Education & Experience
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University degree in statistics, mathematics, mathematical biometrics, or comparable qualification.
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5–10 years of experience in clinical trial statistical evaluation within a CRO or pharmaceutical company.
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Proven project responsibility experience.
Technical Skills
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Strong knowledge of regulatory guidelines and CDISC standards.
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Experience with clinical trial statistical analysis and reporting.
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Familiarity with clinical data standards and regulatory compliance.
Soft Skills
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Excellent verbal and written communication skills.
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Strong customer orientation and high social competence.
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Confident in client interactions and presentations.
What We Offer
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Family-friendly work culture and flexible working options
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Attractive remuneration & benefits
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Flat hierarchy and friendly working environment
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Challenging tasks with regular training and development