FREELANCE: 3 x Statistician - Home Based anywhere in the EMEA

• 6 month rolling contract
• Earliest Start Date: 7th October
• Latest Start Date: December 2019
• Number of positions available: 3
• Home Based anywhere in EMEA

James Carrera has partnered with an international client who is keen to increase both their Early and Late Phase Teams with European based remote workers on a Freelance basis. We can consider prospective candidates based anywhere in the EMEA.

As Principal Statistician you will lead research design and analytical strategies, input into protocols, develop and review statistical analysis plans and author/co-author reports, abstracts and manuscripts and provide statistical advice. You will input into the quality control of statistical deliverables. As the Functional Lead within a study team, you will lead the biostatistical and statistical programming activities on a study and be accountable for the deliverables from these functions. Key responsibilities also include; project management of deliverables, resource and function specific budget. You will have the opportunity to become a subject matter expert for specific tasks within a key client partnership and to become involved in business development activities.

Responsibilities;

• Perform or supervise complex statistical analyses and create or provide input to statistical reports.
• Cooperate with other biostatistical and company departments to optimize global efficiency.
• Act as a pro-active advisor for all types of analysis during the proposal process as well as during the project life cycle; define strategies and evaluate the statistical resources needed to meet the defined goals.
• Coordinate Biostatistics related project activities for successful completion within given timelines and budget.
• Interact with clients with regard to data analysis, scope of work, and budget.
• Review derived datasets and all types of statistical analysis deliverables.
• Develop complex analysis strategies and execute them using efficient programming techniques (software: SAS, R).
• Produce and provide expert input to analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents.
• Quality control of all kinds of statistical deliverables.
• Train/mentor junior members of the department.

Qualifications

• Masters or PhD in a statistical discipline.
• A thorough understanding of the statistical aspects of both clinical trials and observational studies.
• Experience in statistical analysis in a clinically related subject, either within clinical trials.
• Have advanced SAS programming skills, but this is not necessarily essential.
• Strong oral and written English communication skills.