Research, academy jobs in Limuru, Kenya

2 jobs found

IQVIA

Senior Biostatistician

Nairobi

Kenya

Closed for applications
UNEP

Term Review Expert - GF4SL

Nairobi

Kenya

Closed for applications
IQVIA

Senior Biostatistician - Global BIOS (Permanent Homebased)

Nairobi

Kenya

Closed for applications
IQVIA

Global Study Leadership - Clinical Leads

Nairobi

Kenya

Closed for applications
International Centre for Reproductive Health

Mixed-Methods Research Assistant (Qualitative & Quantitative Data Collection)- Nairobi

Nairobi

Kenya

Closed for applications
GiveDirectly, Inc

Senior Research Manager

Nairobi

Kenya

Closed for applications
Shamiri Institute

Associate- Research Management

Nairobi

Kenya

Closed for applications
CloudFactory

Research & Sourcing Specialist

Nairobi

Kenya

Closed for applications
UNEP

Statistics Consultant

Nairobi

Kenya

Closed for applications

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Aga Khan Hospitals

Research Fellow, Bridge, Provost Office CoE

Nairobi

Kenya

Closed for applications
IQVIA

Health care + 1 more

Senior Biostatistician

Closed for applications
Job details

Contract Type

Description

Requirements:

  • BSc or MSc degree in Biostatistics or related field and between 4 - 6 years’ relevant experience
  • Familiarity with moderately complex statistical methods that apply to applicable clinical trials
  • Good working knowledge of SAS and CDISC SDTM and ADaM
  • Ability to effectively manage multiple tasks and project, ability to communicate and explain statistics


Responsibilities
  • As a Senior Biostatistician, you will be given access to cutting-edge, in-house technology and opportunities to work on global projects across a variety of therapeutic areas.
  • You will provide statistical consulting and technical support as it relates to the design, statistical analysis, and regulatory submissions of clinical trial studies.
  • Acting as a statistical team lead for single, complex studies or groups of studies, you will manage the scope of work and budget, providing revenue and resource forecasts, coupled with preparing proposal text and attending bid defense meetings.
  • You will also collaborate with medical and programming staff to produce interim reports and final reports, allowing a comprehensive understanding and interpretation of the clinical trial data and outcome.


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