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Planet Pharma

Senior Statistician

Oxford
Posted 8 days ago
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Senior Statistician

Senior Statistician – Shape the Future of Clinical Innovation

Exciting opportunity to join a dynamic team dedicated to advancing groundbreaking clinical research as a Senior Statistician. Reporting directly to the Director of Biometrics, this pivotal role will see you provide expert statistical guidance across a diverse portfolio of clinical programs, driving impactful research and life-changing therapies in a collaborative environment.

Key Responsibilities

  • Provide expert statistical support across clinical programs
  • Guide data analysis, study design, and regulatory compliance
  • Collaborate with cross-functional teams and vendors
  • Ensure excellence in statistical reporting and analysis

Reasons to use Rodeo

I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?

Honest answer — it depends on where you want to end up. A lot of top grad schemes (Big 4, civil service, banking) don’t need a masters. Let’s look at the ones you’d be competitive for now, and we can decide if a masters actually adds anything.

Also worth knowing: most autumn 2026 applications are open now. Timing matters more than you think.

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Graduate Consultant — 2026 Scheme

PwC·London, UK
£35,000/yr

Why you're a good match

Strong

Your economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.

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Why you're a good match

You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.

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Strong

Experience fit

Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.

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Essential Skills

  • Proven experience applying statistical methods in clinical trials
  • Strong skills in SAS® and R programming
  • Expertise in designing and reviewing statistical analysis plans
  • Knowledge of CDISC standards and clinical data submission processes
  • Ability to coordinate with vendors and cross-functional teams
  • Understanding of GCP regulations and drug development processes

Nice-to-Have Skills

  • Experience in oncology or diagnostic imaging
  • Familiarity with NDA/MAA documentation and regulatory submissions

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Preferred Education & Experience

  • BSc (Hons) in a scientific or mathematical discipline (MSc or PhD preferred)
  • Significant postgraduate experience in statistical roles within clinical research

Additional Requirements

  • Flexibility to work 1 day on-site in Oxford
  • Strong communication skills and ability to prioritise in fast-paced settings

If you’re ready to make an impact in clinical science and thrive in a collaborative environment, apply now to take your career to the next level!

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Skills

Statistical Methods
Clinical Trials
SAS
R Programming
Statistical Analysis Plans
CDISC Standards
Clinical Data Submission
Vendor Coordination
Cross-Functional Teams
GCP Regulations
Drug Development
Oncology Experience
Diagnostic Imaging
NDA Documentation
Regulatory Submissions

Location

Oxford, England, United Kingdom

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