Accessibility Links

Expert Statistician

  • Job type: Permanent
  • Location: Frankfurt am Main
  • Salary: Competitive
  • Job reference: EHOE04121704
  • Sector: Biostatistics, EPM Scientific, Pharmacology
  • Date posted: 04/12/2017
An innovative, leading pioneer and global pharmaceutical company, looking to hire an Expert Statistician to provide statistical support to their rapidly growing team. This role will be located in Frankfurt, Germany; the proposed candidate will use a rigorous statistical methodology to conduct studies, prepare the statistical components of projects in early clinical development and ensure optimisation of early development plan in compliance with procedures and regulations.

Company Overview

The company is one of the most scientifically advanced and leading healthcare organisations in the world, a respected member of the drug development world and a global leader with their established pipeline. They pride themselves on their global reach, with over 100,000 employees globally. This company is dedicated to detecting the root cause of diseases and inventing solutions to enable drug treatment, drug development, drug production and drug manufacturing for the delivery of healthcare products worldwide.

Responsibilities:
  • Contribute to the elaboration of the early development strategy
    • Make proposals to improve designs, analyses and, more broadly, the efficiency and effectiveness of the department through continuous bibliographic monitoring
    • Creation and review of SAPs and contributions to clinical trial protocols and reports
    • Statistical programming (SAS) and review
    • TFL production and review
    • Management of projects and project teams
    • Consulting on statistical and methodological questions
    • Communication with clients and regulatory authorities.
Skills and Experience Required
  • MSc or PhD in Mathematics, Statistics/Biostatistics or Biology (Or equivalent)
    • 4+ Years Biostatistics Experience
    • 3+ Years Pharma or CRO or Academia/Research Institute Experience
    • Extensive Clinical Studies Background
    • Good knowledge of CDISC standards (AdAM) and profound knowledge SAS, SQL and MS-Office
    • Excellent Verbal and written English skills
    • All applicants must be eligible to work in Europe
Package:
  • Competitive benefits and great personal development opportunities
  • Work in the city centre of Frankfurt
    • Great scope for internal career progression
    • A modern and inventive working environment
    • Insight into cutting-edge technologies for the successful development of their pipeline
Apply: If you are interested in this opportunity or if you would like a confidential discussion about your career opportunities please contact: apply.a33ho1gkdcr@epmscientific.aptrack.co.ukor phone +442037588895

Similar jobs
VP Clinical Development- CNS
  • Job type: Permanent
  • Location: Munich
  • Salary: Competitive
  • Description JOB TITLE: VP Clinical Development CNS   A leading Biotech company is seeking an experienced VP of Clinical Development to join their executive management team in...
Medical Director
  • Job type: Permanent
  • Location: Switzerland
  • Salary: £165000 - £220000 per annum
  • Description A fast growing and very exciting biotech with a strong pipeline in the haemophilia and haemtology field is currently looking to add to their medical...
Senior Medical Director
  • Job type: Permanent
  • Location: Zürich
  • Salary: €220000 - €230000 per annum
  • Description The Medical Director will be responsible for medical affairs activities covering Switzerland.  Will be overseeing scientific exchange between healthcare professionals and KOLs within the Oncology
Clinical Director
  • Job type: Permanent
  • Location: Germany
  • Salary: €150000 - €300000 per annum
  • Description This is an opportunity to join a global health care leader currently supporting trials in rare and orphan diseases. They are building a brighter future...
QC Manager
  • Job type: Permanent
  • Location: Brussels
  • Salary: Competitive
  • Description Summary A multiproduct and multi-client site that provides biopharmaceutical manufacturing services. This facility complies with all rules and regulations of current Good