Job Title: Senior Biostatistician - Global Biopharmaceutical
Contract: 12-month contract
Hours: 40 per week
Location: Macclesfield (Remote)
Salary: £72.83 (PAYE) or £77.73 (Umb) per hour
SRG are working with a Global Biopharmaceutical company to help them find a Senior Biostatistician to join their busy team.
The Biostatistics Contractor is a delivery focused role working under the leadership, oversight and direction of assigned Supervisor, responsible for activities relating to design, delivery and interpretation, preclinical studies, regulatory submissions and/or commercialisation. The position requires sufficient experience working as a statistician in the pharmaceutical industry, to be able to independently perform and/or lead statistical work within a study, multiple studies, indication, or be recognised as a methodology expert. This individual is able to support and/or lead work either in house or partnering externally to ensure delivery to standards, quality and time.
Key Responsibilities will include:
- May serve as a supporting or lead statistician for a study, multiple studies, indication within a project (potentially as a Global Product Statistician) or a project-level activity, such as a regulatory or payer submission, responsible for statistical elements of the design, analysis, interpretation and/or reporting,
- Quantifies the benefit, risk, value and uncertainty of the emerging asset/product profile,
- Develops design options and provides high quality deliverables to support the business in making informed decisions,
- Contributes to statistical methodology advances by identifying new opportunities, investigating and applying novel statistical approaches, including modelling and simulation,
- Ensures high quality is built into own and other statisticians' deliverables,
- Ensures compliance with standards and external regulations,
- Contributes to the development of best practices to improve quality, efficiency and effectiveness within function,
- Plans and supports Team's project activities and tasks,
- Communicates and escalates risks within the assigned studies and/or projects,
- Collaborates internally and externally, to ensure delivery to standards, quality and time
Candidate Requirements:
- MSc/PhD in Statistics or Mathematics (containing a substantial statistical component) with experience in pharma industry.
- Good SAS programming skills.
- Thorough knowledge of the technical and regulatory requirements related to the role.
- Experience in the study and/or program design, development, data analysis and interpretation, as well as regulatory interactions and/or submissions.
- Ability to proactively manage concurrent activities within a study or project.
- Ability to apply novel statistical methods to problem solving.
- Ability to manage relevant documentation.
- Excellent communication skills and ability to build strong internal and external relationships.
Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.