Statistics Manager
- Stockley Park, Middlesex (GBR)
- Negotiable
- 12 Months
- Start date: ASAP
- Ref: GSK0JP00075976
- project management
- statistical analysis
- reporting
- clinical trials
- therapy
- sas
- statistician
Job Description
As acting Project Statistician, provide statistical leadership for multiple HIV Phase III/IIIb studies for regulatory submission and post-marketing activities.
Key contributor to the planning and direction of a project and effectively prioritises goals.
Provide statistical contribution when reviewing protocols, statistical analysis plans, reports, publications, and responding to regulatory questions.
Using effective communication and management skills, ensure statistical reporting is robust and delivered on time.
While liaising with Project/Study Programmer(s), coordinates internal & external programming across several studies.
Effectively explains technical concepts and results at all levels in the organisation, including senior managers/stakeholders.
Considered internally and/or externally as a statistical expert in some methodologies.
Makes impactful contributions to internal discussions on emerging statistical methodologies.
Keeps abreast of benchmark data and new research within the therapy area.
Consistently contributes to solving problems for others and proactively considers how solutions could be applied more broadly ensuring knowledge can be captured and reused.
Established track record of generating alternative solutions and perspectives; effectively evaluates advantages and disadvantages.
Promotes new innovations and efficient ways of working.
Accountabilities:
Regular interactions with a broad range of customers.
Plans own and statistical team’s work over multiple projects
Will be a representative on multi-disciplinary teams.
May lead contact for external organizations for projects.
Defines content of study document without supervision.
Defines content of complex documents such as summary documents and regulatory responses without supervision.
Education / Skills:
Masters Degree/Ph.D. required.
Extensive late phase (III/IV) clinical trial and regulatory submission experience required.
Effectively leads and communicates within major projects.
Excellent project management experience as will be working on multiple studies simultaneously.
Raises, discusses and resolves concerns/issues with relevant multi-disciplinary teams.
Applies therapeutic/scientific knowledge to enhance contributions to a project.
Attention to detail.
Experience using SAS, an advantage.
All profiles will be reviewed against the required skills and experience. Due to the high number of applications, we will only be able to respond to successful applicants in the first instance. We thank you for your interest and the time taken to apply.
