Principal Medical & Payer Evidence Statistician

Principal Medical & Payer Evidence Statistician

Cambridgeshire (Remote Working Initially)

6-month contract (high possibility for extension past that point)

Brief

Principal Medical & Payer Evidence Statistician needed for a highly reputable Pharmaceutical organisation based in Cambridgeshire who are looking to employ an experienced and well-rounded Principal Medical & Payer Evidence Statistician takes pride in their work with experience in RWE observational research study management and data analytics, either within pharmaceutical industry or with an observational research consulting firm or academia and extensive knowledge and demonstrated experience with a variety of real-world data sources and observational research study design/execution in biotech/pharmaceuticals, consulting or academia..

What the role entails:

Some of the main duties of the Principal Medical & Payer Evidence Statistician will include:

• Provide statistical expertise in the design, analysis and interpretation of secondary observational research studies/IVS contracts and primary data collection clinical studies/trials in support of BioPharmaceuticals Medical & Payer evidence generation research activities.
• Provide expert advice in the analysis of real-world data (such as medical claims, electronic health records, registries) for stakeholders in Epidemiology, Market Access / HEOR, Medical Affairs, and other functional areas. These analyses may include:

• Treatment patterns and drug utilization
• Resource utilization
• The incidence and prevalence of diseases and co-morbidities
• Cost-effectiveness
• Burden of disease
• Comparative effectiveness and safety
• Value Based Contract Agreements

• Provide statistical guidance on the development of Study Design Concepts, Protocols, Statistical Analysis Plans, Data Presentation Plans, Clinical Study Reports and publication activities in support of BPM clinical/observational study activities.
• Provide oversight of CRO analytic activities for outsourced BPM clinical/observational studies as needed, supporting the Study Lead in reviewing all analytical activities outsourced to external vendors, including analysis plans, review of interim/final results and publications development.
• May provide hands-on analytical support for internal RWE analyses across BioPharmaceuticals Medical.
• Collaborate in the development of operational systems and research processes to increase the effectiveness and efficiency of BPM Evidence and RWS&D research efforts.

What experience you need to be the successful Principal Medical & Payer Evidence Statistician:

• Graduate degree in Statistics, Biostatistics, or related quantitative fields (epidemiology, health outcomes, health informatics or health economics) or equivalent course work/ technical experience with experience in pharma/healthcare or other relevant discipline.
• MS with 5 years of experience or PhD with 2 years of experience in the design, analysis and reporting of clinical studies/trials in a pharmaceutical research or academic setting.
• At least 3+ years-experience in RWE observational research study management and data analytics, either within pharmaceutical industry or with an observational research consulting firm or academia.
• Extensive knowledge and demonstrated experience with a variety of real-world data sources and observational research study design/execution in biotech/pharmaceuticals, consulting or academia.

This really is a fantastic opportunity for a Principal Medical & Payer Evidence Statistician to progress their career. If you are interested please apply as soon as possible as this position will be filled quickly so don't miss out!

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