Senior Biostatistician

Description:

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