Global Study Manager/Lead responsible for end-to-end clinical study delivery, budgeting, risk management, and stakeholder communication across multiple regions.
Responsibilities
Accountable for operational delivery of clinical studies to time, quality, and budget
Generate robust delivery plans and deliver to target thresholds
Lead study team and matrix teams
Develop protocol and informed consent documents
Conduct investigator meetings and other study related meetings
Requirements
Bachelor’s degree in life sciences or related discipline
Seeking experienced Senior Statistical Programmers to join the Biometrics Partnership to deliver statistical programming activities across clinical studies, supporting analysis, and regulatory submissions.
Locations (4)
Johannesburg, Gauteng, South Africa
Kenya
Poland
Hungary
Responsibilities
Develop, validate, and maintain complex SAS and R programs for clinical trial analysis and reporting
Lead statistical programming activities for assigned studies, ensuring high-quality and timely delivery
Create and review ADaM datasets, Tables, Listings and Figures (TLFs), and associated programming specifications
Collaborate with statisticians, data managers, and cross-functional study teams to deliver regulatory-compliant outputs
Support submission activities including Define.xml and other regulatory deliverables
Requirements
Bachelor's degree in Statistics, Mathematics, Computer Science, Life Sciences, or a related discipline