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Principal Biostatistician

Remote: 
Full Remote
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

Master’s degree in statistics or biostatistics required, Minimum of 8 years of biostatistical experience desired, Clinical experience is mandatory, Expertise in multiple statistical areas and SAS procedures.

Key responsabilities:

  • Perform Study Statistician role with minimal supervision
  • Support design, analysis, and interpretation of clinical trials

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KCR Placement http://www.kcrplacement.com
11 - 50 Employees
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Job description

KCR Placement is a full-service functional sourcing and recruitment provider. As part of the ICON organization, we specialize in high-speed and high-quality talent sourcing for the CRO, Pharmaceutical, Biotech and Medical Device industries across Europe.

Our employees are KCR Placement's most crucial asset. We commit to placing our candidates at the center of all we do and prepare them for long-term career development and success with competitive benefits and vibrant work environment. The KCR Placement team is supported by a specialized referral network of expert professionals and is dedicated to providing sourcing services and client support from job requisition to job offer.


We are currently looking for highly experienced Biostatisticians to join our growing structure of international FSP and FSO Services due to new trials and development of clients portfolio. Interesting studies, possibilities to adjust to your expectations as per clinical career development.


As a Principal Statistician you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.


Title: Principal Biostatistician 


Location: UK, Bulgaria, Poland, Romania, Hungary


Duties associated with the role include:

  • 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, 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


Requirements:

  • 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


To show that you are appreciated in our team, you will be provided with:

  • 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


Our Privacy Policy

As KCR became part of the ICON group, your personal data will be shared with ICON and processed in accordance with privacy notice: https://www.iconplc.com/privacy/job-applicants

If you want your candidacy to be considered also for future recruitments, please send us an additional consent: “I agree to the processing of my personal data for any future recruitments conducted by ICON”. Such consent may be placed in your CV or electronic correspondence addressed to us. You can withdraw your consent at any time. Withdrawal of consent does not affect the legality of the processing carried out prior to its withdrawal.


KCR is an equal opportunity employer. In line with our motto, ‘We see human behind every number,’ KCR is committed to fostering an inclusive culture and maintaining a diverse, safe, and respectful working environment with equitable treatment for all.

We are committed to non-discriminatory practices and provide an equal opportunity for all qualified employees and job applicants within all employment sectors. We believe that in developing a desirable culture of belonging in which diverse perspectives and voices are welcomed and heard, the full potential of employees can be achieved.


Required profile

Experience

Level of experience: Senior (5-10 years)
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Quality Control
  • Teamwork
  • Communication
  • Problem Solving

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