Statistical Scientist - Basel, Schweiz - CTC Resourcing Solutions

CTC Resourcing Solutions
CTC Resourcing Solutions
Geprüftes Unternehmen
Basel, Schweiz

vor 2 Wochen

Lena Schneider

Geschrieben von:

Lena Schneider

beBee Recruiter


Beschreibung

_The Life Science Career Network_

Statistical Scientist
Our client is a pioneer in Drug Discovery and Development and one of the frontrunners in Personalised Healthcare.

As the world's largest R&D spender in the pharmaceutical and diagnostics domain, they work in a vast number of drug discovery & therapeutic areas and are highly recognized internationally.


We are currently looking for a Statistical Scientist for a
12-month contract (with high possibility for extension) based in Basel, Switzerland.



Main Responsibilities:


  • Clinical Study and observational study Planning: in collaboration with Senior Statistical Data Scientists, reviews study protocols, authors statistical sections of protocols.
  • In collaboration with Senior Statistical Scientists, develops independent data monitoring and endpoint committee charters.
  • Development of the statistical and data analysis plans, and preparation of the study randomization.
  • Study Conduct: reviews case report forms to ensure protocol objectives are met and project standards are maintained.
  • Development of statistical programs as necessary to perform analyses, review analyses produced by statistical programming, ensuring the accuracy & validity of results.
  • Clinical/observational study Analysis & Reporting: author the clinical study report, In collaboration with Senior Statistical Scientists and crossfunctional team members, provides input into global health authority documents and regulatory response for health authority submissions.

Qualifications and Experience:

-
_Relevant working/residency permit or Swiss/EU-Citizenship required_:

  • MSc or PhD in Statistics, Biostatistics, Mathematics or similar areas of academic discipline
  • Minimum of 3 years of experience as a clinical study statistician
  • Experience in Running, planning and interpreting clinical trial data
  • 3 years of Experience in using statistical software SAS or R
  • Good knowledge of theoretical and applied statistics.
  • Good knowledge of English in a business environment.

Nice to Have:

  • Project management skills (including ability to manage scope and effectively delegate to other functions, staff, contractors and external vendors).
  • Strategic Agility (including problemsolving and critical thinking skills, ability to drive drug development strategies, agility that extends beyond statistical aspects).
  • Prior experience with SaMD Launch preferable but not mandatory

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