Principal Biostatistician

ProClinical is partnering with a leading multinational contract research organisation to advertise a vacancy for a Principal Biostatistician position. The organisation is one of the world's forefront innovators in biopharmaceutical services, providing high quality Phase I-IV clinical research, regulatory, consulting, and market access services. The position will be based in the company's Munich office. These vacancies offer an exciting opportunity to work with a prestigious CRO that pioneers drug development.

Job Responsibilities:

• Performing or supervising complex statistical analyses and creating or providing input to statistical reports.
• Cooperating with other departments to optimise the global efficiency.
• Acting as a pro-active advisor for all types of analysis during the proposal process as well as during the project life cycle; defining strategies and evaluating the statistical resources needed to meet the defined goals.
• Coordinating Biostatistics related project activities for the successful completion within given timelines and budget.
• Interacting with clients regarding data analysis, scope of work, and budget.
• Reviewing derived datasets and all types of statistical analysis deliverables.
• Developing complex analysis strategies and executing them using efficient programming techniques, such as with SAS software.
• Producing and providing expert input to analysis plans, statistical reports, statistical sections of integrated clinical reports, and other process supporting documents.
• Overseeing Quality Control of all kinds of statistical deliverables.
• Training/mentoring junior members of the department.

Skills and Requirements:

• A degree in Biostatistics/Statistics or relevant quantitative sciences degree.
• A Masters or PhD in a statistical subject.
• A thorough understanding of statistical issues in both clinical trials (and other randomised experiments) and observational studies, (. e.g. comparative cohort studies, case-control, retrospective/prospective cohort).
• Experience in statistical analysis in a clinically related subject, either within clinical trials or in Epidemiology, either academically or professional, and/or Outcomes research.
• Experience with oncology and/or diabetes trials would be an advantage.
• Advanced SAS programming skills.
• Good business awareness/business development skills, including financial awareness.
• Demonstrable multitasking, project management, and execution skills.
• Good interpersonal skills, including communication, presentation, persuasion, and influence.
• Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
• Proficiency with computer skills, such as MS Office.

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Theodora Savlovschi-Wicks at +44 203 752 0314 or upload your CV on our website - www.proclinical.com.

A full job description is available on request.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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