Senior Statistician

at  ICON

Home Based, KwaZulu-Natal, South Africa -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate25 Jun, 2024Not Specified26 Mar, 20248 year(s) or aboveGood communication skillsNoNo
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Description:

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

WHAT ICON CAN OFFER YOU:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles

Responsibilities:

  • Ability to perform Study Statistician role with minimal supervision
  • Demonstrates strong statistical expertise with a good understanding of more complex design of experiments and inference methodologies (where applicable awareness / knowledge of Bayesian, Futility &
  • Predictive Inference, Estimands, Missing Data etc.)
  • Where required, ability to actively participate in matrix team meetings
  • Applies standard processes to tasks, ensuring that deliverables are accurate, high quality and met according to agreed timelines
  • Extensive working knowledge of GxP, ICH, internal GSK processes and external regulations (as applicable)
  • Quality Control (QC) of other people’s work under supervision
  • Under supervision:
  • Supports design, analysis and interpretation, uses a wide range of statistical approaches and/or applicable software to explore options
  • Authors analysis plans and prepares statistical inputs to key documents and presentation materials
  • Contributes to the development of statistical strategy at a study-level, which may be shared with stakeholders

You are:

  • Master’s degree in statistics or biostatistics required.
  • Minimum of 8 years of biostatistical experience desired.
  • Clinical experience is mandatory
  • Exhibit expertise in multiple statistical areas, the drug development process, SAS procedures and good programming practices.
  • Thorough knowledge of and experience with CDISC standards is desired.
  • Demonstrate ability to plan, supervise, implement and monitor the statistical processes for multiple clinical trials.
  • Knowledge of ICH-GCP and other applicable legislation to successfully execute the clinical study.
  • Auto-immune and/or oncology clinical study background is a plus.
  • Experience in managing vendors is a plus


REQUIREMENT SUMMARY

Min:8.0Max:13.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

Home Based, South Africa