Statistician Work, Jobs in Radley, Oxf (with Salaries)

Senior Statistician
PSI CRO —Oxford
- Full-time
- Remote
- English
- Master's degree
- Quality control
Quick apply
Principal Statistician (Pharmacokinetics)
PSI CRO —Oxford
- Full-time
- Remote
- English
- Master's degree
- Communication skills
Quick apply
Principal Statistician
PSI CRO —Oxford
- Full-time
- Remote
- Master's degree
- Communication skills
Quick apply
Statistical Programmer
University of Oxford —Oxford
- £39,424 - £47,779 a year
- Full-time
- Epic
Critical Care Research Group Operational Lead
University of Oxford —Oxford
- £49,119 - £58,265 a year
- Full-time
- Doctoral degree
7d
Postdoctoral Research Scientist in host genetics and data integration for liver cancer risk predication and early detection
University of Oxford —Oxford
- £39,424 - £47,779 a year
- Full-time
- Doctoral degree
- Research
- University
- Annual leave
- Employee discount
4h
Principal Statistical Programmer - FSP (Permanent Homebased) m/w/d
IQVIA —Reading
- Full-time
- Remote
- Computer Science
- Bachelor's degree
- Training & development
- Work from home
Statistics & Analysis Manager
Abbott Laboratories —Witney
- Full-time
- Team management
- Training & development
- Leadership

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Research Assistant
University of Oxford —Oxford
Applicants will need to hold a degree in Genetics, Neuroscience, Translational Research, or related subjects. In addition, experience gained by supervision and…
£35,681 - £46,476 a year
10d
Clinical Trials Research Assistant
University of Oxford —Oxford
The position would also include support of ongoing clinical trial activities including sample processing, general lab duties (maintaining supplies, consumables…
£35,681 - £41,636 a year
10d

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Senior Statistician

PSI CRO -
Oxford

Quick apply

Job details

Full-time

Qualifications

Project quality assurance reviews
Statistics
Clinical research
SAS
Stakeholder liaison
English
Master's degree
Statistical analysis
Quality control

Full job description

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

In this role, you will:

Lead all biostatistics activities related to clinical trials as responsible project statistician
Communicate with project teams, clients and vendors on statistical questions
Develop and review statistical sections of protocols, including sample size calculations
Develop statistical analysis plans
Develop and document analysis database structures (i.e. SAS analysis data set structures)
Develop SAS program requirements and specifications
SAS programming and program validation
Review and QC of statistical deliverables (tables, listings, figures, etc.)
Perform statistical analysis and report results
Consult on experimental design, statistical methods and approaches for the purpose of assessing safety and efficacy of drug products
Liaise with DM on statistical questions related to data issues, including coordination of data transfers from DM to Statistics
Participate in bid defense meetings and kick-off meetings
Train statisticians and SAS programmers
Prepare and deliver presentations at investigators' meetings
Address audits findings/recommendations, and follow-up on and resolution of audit findings

Qualifications

MSc in Statistics or equivalent
Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research
Ability to apply a range of advanced statistical techniques in support of clinical research studies and to analyze, interpret, and draw conclusions from complex statistical information
Ability to consult with clinical investigators, interpret research requirements, and determine statistical analysis strategies
Expert knowledge and understanding of the SAS programming
Expert knowledge and understanding of CDISC ADaM standard
Knowledge of relevant regulations and guidelines (e.g. FDA, EMA, ICH)
Ability to work in English

Additional Information

Our mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way.

Quick apply

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statistician jobs in radley, oxf

Senior Statistician

Principal Statistician (Pharmacokinetics)

Principal Statistician

Statistical Programmer

Critical Care Research Group Operational Lead

Postdoctoral Research Scientist in host genetics and data integration for liver cancer risk predication and early detection

Principal Statistical Programmer - FSP (Permanent Homebased) m/w/d

Statistics & Analysis Manager

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