Senior Biostatistiker:in

SimplyVision GmbH; Basel; Hybrid; CHF 100’000 - 125’000; Vollzeit

Zusammenfassung

An innovative firm is seeking a Senior Principal Biostatistician to lead statistical efforts in clinical trials. This role offers the chance to work independently and collaboratively on complex statistical tasks while contributing to drug development projects. You will engage with cross-functional teams, utilizing your statistical expertise to influence project outcomes. Your ability to communicate complex statistical concepts clearly will be essential as you work with both statisticians and non-statisticians. Join a dynamic team where your contributions will directly impact clinical research and enhance patient outcomes.

Qualifikationen

• 3+ years relevant work experience with a Master's or 1+ years with a PhD in Statistics.
• Proficiency in statistical software packages like SAS and R.

Aufgaben

• Responsible for all statistical tasks on assigned clinical trials independently.
• Develop statistical analysis plans and ensure timely delivery of Biostatistics deliverables.

Kenntnisse

Statistical Analysis

Communication Skills

Project Management

Data Exploration

Machine Learning

Data Visualization

Ausbildung

Master's in Statistics or equivalent

PhD in Statistics or equivalent

Tools

SAS

R

Jobbeschreibung

For our customer located in Basel/Switzerland we are currently looking for a: Senior Principal Biostatistician (m/f/d)

• Location: Basel and remote
• Branch: Pharma
• Duration: 12 Months contract
• pay rate range: 68,58 – 97,48 chf/h (given by client): typical monthly gross salary, e.g. 160h*70 chf/h gross = 11.200 chf gross/month

Tasks & Responsibilities

The Senior Principal Biostatistician is responsible and accountable for all statistical work, scientific and operational, for one or more assigned clinical trials in collaboration with the clinical trial team/global clinical team. You will work independently at the clinical trial level and may lead project level statistical activities for a drug development project under limited supervision. You will be responsible of statistical models, analysis and data exploration methodologies at the study or project level.

• Responsible for all statistical tasks on the assigned clinical trials and perform these tasks for mid- to high complexity trials independently with peer review/input as required. Responsible for developing statistical analysis plan, study and indication-level reporting activities.
• Contribute to planning and execution of exploratory analyses to support publication activities. Initiate and implement novel methods for exploratory analyses in alignment with the Lead Statistician (like Machine Learning and Data Visualization).
• Explain statistical methodology and interpret analysis results. Provide statistical expertise to support the teams and significantly contributing to meetings. Contribute to interactions with external investigators (as needed).
• Represent the Biostatistics Line Function on cross-functional teams for the assigned trials. Responsible for functional alignment and ensuring line function awareness throughout the trials.
• Collaborate with other line functions. Explain statistical concepts in an easily understandable way to non-statisticians and provide adequate statistical justifications for actions/decisions/statements, when required.
• Establish and maintain collaborative relationships and effective communications cross functionally within the Clinical Trial Team and Biostatistics team.
• Ensure all Biostatistics deliverables (as SAP, analyses) for assigned clinical trials and/or non-clinical related activities are delivered in a timely manner with the highest level of quality.

Must Haves

• MS (in Statistics or equivalent) with 3+ years relevant work experience or PhD (in Statistics or equivalent) with 1+ years’ relevant work experience.
• Fluent in English with strong communication and presentation skills.
• Previous client experience is essential
• Influences decisions that directly impact the trial/project and team ability to deliver objectives.
• Demonstrable experience in all tasks of a statistician at trial and experiment level with the ability to work independently. Demonstrable knowledge and expertise in statistics and its application to clinical trials; ability to explain statistical designs and concepts. Depending on the assignment, may require proven expertise in data exploration skills.
• Proficiency in use of statistical software packages (e.g. SAS, R).
• Good knowledge of drug development and Health Authority guidelines.
• Demonstrated efficiency working on a multidisciplinary team to achieve team objectives.
• Good project management skills and ability to collaborate well with non-statistical functions.