Position Purpose The Associate Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory obligations. The individual will work closely with
Main Responsibilities: Responsible for the implementation and use of programs to effectively analyze and report clinical trial data as the trial programmer. Responsible for the review of trial documentation and providing feedback from statistical programming perspective, as
The Senior Statistical Programmer is responsible for providing hands-on support and technical guidance on clinical study teams. The development of study and ad hoc output, including, but not limited to: ADaM datasets, tables, figures, and listings output
Our client is headquartered in Switzerland – a biotech-hub of Europe – is a high-potential biopharmaceutical company, specialized in the discovery, development and commercialization of innovative small molecules, with the aim of transforming the horizon of
VIATRIS INNOVATION GMBH At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions, and is accountable for the statistical deliverables within
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable for the statistical deliverables within
Main Responsibilities: Ensures that Data Management (Biometry) activities (related to assigned trial) adhere to the company Standards, and applicable regulations Meets trial timelines in terms of Data Management deliverables Ensures data handling consistency within allocated trial(s)
Our client, a high‑potential biopharmaceutical company headquartered in Switzerland, is looking for a Trial Data Manager for an initial 24‑month contract based in the Basel area. Trial Data Manager leads Data Management activities for assigned trials and
Our client is headquartered in Switzerland – a biotech-hub of Europe – is a high-potential biopharmaceutical company, specialized in the discovery, development and commercialization of innovative small molecules, with the aim of transforming the horizon of
Job Description You will contribute to statistical activities related to global clinical trials and work closely with international teams of statisticians, programmers and data managers, including the role of biostatistics project lead. In this role, you will: Act