Senior or Principal Biostatistician
Location | Europe |
Discipline: | Biometrics |
Job type: | Permanent |
Salary: | £Salary: On application |
Contact name: | Geoff King |
Contact email: | geoff.king@rbwconsulting.com |
Contact phone: | 01293584300 |
Job ref: | 12345/2/2 |
Published: | almost 3 years ago |
Expiry date: | 10 Jun 2021 11:59 |
Location: Home based UK and Europe
Geoff King at RBW Consulting is working with the world’s largest biometric specialist Clinical Research Organisation (CRO) in the recruitment of multiple Senior or Principal Biostatisticians to join their Flexible Service Provider team as they continue to support a number of the world’s largest pharmaceutical and cutting-edge biotechnology companies.
As a Senior or Principal Biostatistician, you will have the opportunity to work with a high-profile sponsor across a range of studies on multiple therapeutic areas in phase I-IV clinical trials. Fully home based in UK, Ireland, Spain, Germany, France and Switzerland.
For over 30 years this specialist CRO has focused on delivering high quality biostatistics and programming support to life science companies across the globe and now boast offices in the UK, Europe, America and India as a world leader in their field.
Priding themselves in career development, training and an incredibly supportive management team the company continue to go from strength to strength seeing business growth throughout 2020 and continued staffing needs required throughout 2021 due to a number of new studies and sponsors being secured.
Main duties & responsibilities:
Development of study protocols, including participation in study design discussions and sample size calculations
Reviewing CRFs and data review guidelines; developing statistical analysis plans (SAPs), including analysis dataset and TLG specifications
Performing statistical analyses and interpreting statistical results
Preparing clinical study reports, including integrated summaries for submissions (ISS/ISE), other documents for Health Authorities, Publication or exploratory purpose
Leading study activities when called upon
Perform QC and oversight of other third parties' contributions as appropriate
Key requirements:
BSc in Statistics/Biostatistics (or equivalent).
At least 6 years of relevant industry experience.
Understanding of clinical drug development process, relevant disease areas, endpoints and different study designs.
Awareness of industry and project standards & ICH guidelines.
Excellent verbal and written communication skills.
A comprehensive job description is available upon request.
To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Geoff King on +44 (0) 1293 584 300 and send your CV through to geoff.king@rbwconsulting.com or use the apply button on this page.
Salary: Competitive
Latest jobs
- Scientist II - QC Microbiology
-
Job location: New Jersey Job salary: £Up to $90k
Scientist II – QC MicrobiologyPartnering with ...
- Senior Validation Engineer
-
Job location: New Jersey Job salary: £Up to $110k
Senior Validation EngineerAre you a validation...
- Clinical Trial Assistant (CTA)
-
Job location: Greater London Job salary: £35000 to £42000
Role: Clinical Trial Assistant (CTA / Associat...