Clinical Data Analyst/Statistician at Santhera Pharmaceuticals

Pratteln

Key information

Publication date:18 February 2025
Workload:100%
Contract type:Unlimited employment
Place of work:Pratteln

Job summary

Santhera Pharmaceuticals is a Swiss specialty firm focused on rare diseases. Join us to impact lives and advance treatment options.

Tasks

Lead the Biostatistics team and oversee statistical methodologies.
Act as Program Statistician in drug development and regulatory submissions.
Manage and develop biostatistics processes and team oversight.

Skills

M.Sc. in statistics/life sciences with 10+ years in the field.
Expertise in clinical study design and regulatory documentation.
Strong communication skills and understanding of statistical methods.

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Santhera Pharmaceuticals is a Swiss specialty pharmaceutical company focused on medical science and the development and commercialization of innovative pharmaceutical products for the treatment of rare neuromuscular diseases with high unmet medical need. For further information, please visit the Company's website www.santhera.com Come and join our team to contribute to providing treatment options for patients with rare diseases that have a severe impact on the lives of affected children and adults. You can make a difference as:
Head Biostatistics
Location: Pratteln, Switzerland (Hybrid) Scope of Work
As the Head of Biostatistics, you will be a key leader in our growing biotechnology company, responsible for shaping and executing the statistical strategy across our Clinical Development, Regulatory Affairs, Medical Affairs and Medical- Marketing functions. You will lead a multi-disciplinary Biostatistics Department, including statisticians, data managers, and programmers, while ensuring the seamless integration of external vendors and contract research organizations (CROs). This role provides a unique opportunity to make a high impact in a dynamic, fast-paced environment focused on rare diseases in a company with ambitions for growth. You will oversee all statistical aspects of clinical trials and real-world evidence (RWE) studies, ensuring scientific rigor, efficiency, and regulatory compliance. Your role will balance strategic leadership with hands-on expertise, fostering a high-performance team that is data-driven and outcome-focused. Key Responsibilities
Leadership & Strategy
- Define and implement the statistical strategy supporting clinical development and real-world evidence (RWE)studies and initiatives.

Assess and optimize the departmental structure, workflows, and resourcing to ensure efficiency and timely execution of statistical deliverables.

Act as the strategic statistical lead for clinical programs, regulatory submissions, and cross-functional collaborations.

Recruit, retain and mentor talent

Operational Oversight

Provide line management, mentorship, and technical guidance to biostatisticians, data managers, and programmers.

Oversee external vendors and ensure quality delivery of outsourced statistical activities.

Ensure seamless integration of statistical deliverables with clinical and regulatory strategies.

Scientific & Technical Excellence

Lead the development and review of Statistical Analysis Plans (SAPs), study concepts, study protocols, and regulatory documents.

Provide expertise in advanced statistical methodologies, including Bayesian modelling, mixed models, and adaptive trial designs.

Ensure statistical integrity in clinical trials with small sample sizes, typical of rare disease drug development.

Experienced in using SAS

Regulatory & Compliance

Represent the company in global regulatory interactions, including FDA, EMA, and other health authorities.

Contribute to regulatory filings, including NDA/BLA submissions, briefing documents, and responses to agency queries.

Stay ahead of industry trends and evolving statistical methodologies in drug development.

Budget & Resource Management

Develop and maintain departmental forecast and resource plan, ensuring alignment with project goals, timelines and financial targets.

Optimize resource allocation between in-house and outsourced statistical activities.

Required Qualifications & Experience

MSc or PhD in Statistics, Biostatistics, or a related field.

10+ years of experience in clinical biostatistics, with significant exposure to rare diseases, real-world evidence, and regulatory submissions.

5+ years of leadership or cross functional matrix experience, with a proven track record of managing and developing or working within high-performing teams.

Extensive experience in designing clinical studies, including adaptive designs and Bayesian methods;

Regulatory submissions, including NDA/BLA filings and regulatory agency interactions; Advanced statistical modelling, including longitudinal and mixed models; Real-world data analysis and evidence generation strategies; Strong knowledge of GCP, ICH guidelines, and CDISC standards (SDTM, ADaM). Required Competencies & Skills

Excellent communication skills, with the ability to translate complex statistical concepts into actionable insights for cross-functional teams.

Solution-oriented, proactive, and adaptable in dynamic situations.

Fluency in English (additional languages are a plus).

For this position, the relevant working/residency permit or Swiss/EU-Citizenship is required. If you are interested in a multicultural, challenging, and innovative working environment and your profile matches our requirements, we are looking forward to receiving your online application in English via LinkedIn or Email, at E-Mail schreiben Note for agencies: Recruitment agencies are kindly invited to refrain from sending unsolicited CVs to Santhera.