Job Ref: J31774
Sector: Clinical
Sub-sectors: Biotech/Life Sciences, Pharmaceuticals
Job Type: Permanent
Date Added: 03 May 2019
  • London, England, UK Vintners Place, 68 Upper Thames St, London London London UK EC4V 3BJ
  • £35,000 - £65,000 per Annum
  • Jessica Wheeler

Quick Apply

Submitting application, please wait..

Request a callback

Send To A Friend

Biostatistician Mid-sized CRO Full-Time, Perm LondonApprox. £35-65,000 DOE and level SRG are currently recruiting on behalf of a mid-sized Clinical Research Organisation who are looking to grow their UK based biometrics team with a further two Biostatisticians based out of their London office. Ideally they are looking for Clinical Trial experience from within a CRO or Pharma environment however we are also keen to hear from Biotech, Med Devices, Hospital or Clinical Trials Unit biostatisticians. You would be joining a small but growing team that is based in both the UK & US with a main focus on reviewing analysis plans for appropriate methods and providing statistical support/trouble-shooting on all product and process quality issues and more. About the Company: Global full-service organisation with a vibrant open plan environment and a core value of investing into talent and helping their employees to achieve their full potential. It's a fast pace environment and you will be experience hands on, varied tasks which gives you an opportunity to build upon experience within clinical trials. They also offer an attractive salary and benefits package depending on experience and level - which are very market competitive. Responsibilities:* Contribute to clinical trial plan preparation;* Review of study protocol;* Preparation of statistical methodologies;* Programming of study analysis, review of study results and preparation of statistical methods section for clinical / statistical reports;* Communicate project requirements for CRF design, database design and database cleanup to ensure the key study variables are suitable for analysis;* Converse statistical results to medical writing personnel to ensure accurate interpretation. Essential Skills: * MSc. or Ph.D. in Statistics or Biostatistics* SAS Programming experience* Previous experience in a pharmaceutical or CRO setting* Knowledge of advanced statistical methods* Knowledge of regulatory requirements/guidelines for drug development;* The right person should have a passion for Statistics and should want to develop their career in clinical trials * Must be eligible to live and work in the UK (please check before you apply to this role) Please contact Jessica for more details about this role, 0203 960 3548 /

02/06/2019 15:46:51
GBP 35000.00 35000.00