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- Competitive salary
About Our Client
Join a specialist contract research organisation (CRO) based in the UK, with multiple UK offices. They focus on delivering statistics and programming for the reporting of Phase I-IV clinical trials across a variety of therapeutic areas. A respected company, boasting contracts with some of the top 10 pharma companies globally. They offer flexible working and an industry leading training programme
Job Description
Key Responsibilities:
Review clinical trial documents; SAPs, CRFs, CSRs
Program and QC TFLs
Apply statistical techniques; advance survival, non-linear modelling etc
Maintain study master file documents
Lead study team meetings
As a Principal, lead and project manage teams and projects
The Successful Applicant
The Successful Applicant
Relevant qualification - PhD or MSc
Proven experience within industry in a CRO, Biotech/Biopharma or a pharmaceutical company
Demonstrated problem solving skills
Excellent verbal and written communication skills
Project management/lead experience is a plus but not a must have
What's on Offer
What's on Offer
You will have the opportunity to work directly with an FSP client, with no more than 2 clients at one time, maximum. You will have the option to work with 1 client for 100% of your time or a mixture dependant on your preference. As a Senior or Principal Statistician oyou will have the opportunity to be mentored by industry leaders. You will receive a competitive package and the flexibility you need to achieve the right work life balance for you and your family.
Job summary
- Sector
- Life Sciences
- Subsector
- Biometrics
- Sector
- Healthcare / Pharmaceutical
- Location
- England
- Contract type
- Permanent
- Consultant name
- Hajera Sama
- Consultant phone
- +442072692232
- Job reference
- JN-052022-5599147