Senior Biostatistician
IQVIA
Athens, Greece
πριν από 1 μέρα

We are currently looking for a Senior Biostatistician to join our Biostatistician team to work on interesting and innovative projects with similar minded people, the best experts in the field of biostatistics.

You will be able to bring new ideas and be challenged in a highly motivational, multinational environment. With the right support you will be able to follow your personal development path in the direction you choose.

Key responsibilities will include :

Developing statistical methods sections of protocols and reviewing case report forms (CRFs).

Preparing analysis plans and write specifications for analysis files, tables, and figures.

Communicating with clients regarding study protocol or statistical analysis issues as they arise.

Communicating with study team members regarding study execution as it relates to timelines, data quality, and interpretation of results.

Interpreting analyses and write statistical sections of study reports.

Being accountable for controlling costs and maximizing revenue recognition.

Providing training, guidance and mentorship to lower level and new staff.

Qualifications

  • Bachelor's Degree Biostatistics or related field and 3 - 5 years relevant experience
  • Master's Degree Biostatistics or related field and 3-5 years relevant experience
  • Ph.D. Biostatistics or related field and 1 year relevant experience
  • Typically requires 3-5 years of prior relevant experience, or equivalent combination of education, training and experience
  • Requires advanced knowledge of job area, and broad knowledge of a other related job areas, typically obtained through advanced education combined with experience
  • Excellent written and oral communication skills including grammatical / technical writing skills
  • Excellent attention and accuracy with details
  • In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Familiarity with moderately complex statistical methods that apply to applicable clinical trials
  • Strong individual initiative
  • Strong organizing skills
  • Strong working knowledge of SAS computing package
  • Familiarity with other relevant statistical computing packages such as nQuery
  • Strong commitment to quality
  • Ability to effectively manage multiple tasks and projects
  • Ability to lead and co-ordinate small teams
  • Ability to solve moderately complex problems
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients
  • Working knowledge of relevant Data Standards (such as Clinical Data Interchange Standards Consortium CDISC / ADaM)
  • Αναφορά αυτής της εργασίας
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