Statistics — Interview Questions¶
Questions covering central tendency, spread, distributions, hypothesis testing, and A/B testing. These appear in data analyst and product analytics interviews at all levels.
[Beginner] What is the difference between mean, median, and mode? When would you use each?
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- Mean: arithmetic average — affected by outliers. Use when distribution is symmetric.
- Median: middle value — robust to outliers. Use when distribution is skewed (e.g., revenue, income).
- Mode: most common value. Use for categorical data or when the most frequent value is meaningful.
Rule of thumb: if mean and median are far apart (ratio > 1.3), the distribution is skewed and median is more representative. Report both with an explanation.
[Beginner] What is a p-value? What does p = 0.04 mean?
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A p-value is the probability of observing a result as extreme as (or more extreme than) the one you observed, assuming the null hypothesis is true.
p = 0.04 means: if there were truly no effect (H₀), you'd only see a result this extreme 4% of the time by random chance.
At a significance level of α = 0.05, p = 0.04 < 0.05, so you reject H₀ — there is statistically significant evidence of an effect.
Common mistake: p = 0.04 does NOT mean "there's a 96% probability the effect is real." That would be the posterior probability and requires Bayesian reasoning.
[Mid-level] What is the Central Limit Theorem and why does it matter for hypothesis testing?
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The CLT states that the distribution of sample means approaches a normal distribution as sample size increases — regardless of the shape of the underlying population distribution.
Why it matters: - Most hypothesis tests (t-test, z-test) assume the sampling distribution of the mean is normal - The CLT justifies this assumption for large samples (n > 30) even when raw data is skewed - This is why t-tests work on revenue data even though revenue is right-skewed — we're testing means, not individual values
[Mid-level] An A/B test on a new checkout button shows a 3% absolute improvement in conversion rate with p = 0.03. The product manager wants to roll out immediately. What questions do you ask first?
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Sample size and duration: How many users were in each group? How long did the test run? A 3% lift with n=50 per group is unreliable; n=5000 is much stronger.
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Confidence interval: What's the CI for the 3% lift? If it's 0.5%-5.5%, the uncertainty is too wide to make a confident decision.
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Practical significance: Is 3% absolute lift worth the engineering cost to ship? What's the revenue impact if we scale? (3% × 100,000 monthly visitors × average order value = ?)
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Novelty effect: Did we run the test long enough to rule out users being curious about the new button?
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Segment consistency: Did the lift hold across key segments (mobile vs desktop, new vs returning users)? If only one segment improved and others got worse, the overall number is misleading.
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Guardrail metrics: Did any other metrics worsen? (e.g., revenue per conversion, return rate)
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Was the test properly randomised? No interference between groups (e.g., users in both groups)?
[Mid-level] What is the difference between statistical significance and practical significance?
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Statistical significance (low p-value): the observed result is unlikely to be due to random chance.
Practical significance: the effect is large enough to matter for the business.
A result can be: - Statistically significant but practically meaningless: with 1 million users, a 0.01% improvement in conversion is statistically detectable but generates £50/year — not worth building. - Practically significant but not statistically significant: a 10% improvement in a small study (n=30) might not reach p < 0.05 but could be worth running a larger test.
Always report effect size alongside the p-value:
[Senior] You're designing an A/B test to detect a 2% absolute improvement in conversion rate (baseline 12%). Walk me through how you'd determine the required sample size.
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from statsmodels.stats.power import NormalIndPower
import numpy as np
baseline = 0.12 # current conversion rate
effect = 0.02 # minimum detectable effect (absolute)
alpha = 0.05 # significance level (5% false positive rate)
power = 0.80 # 80% chance of detecting a real effect
# Effect size (Cohen's h or standard proportion test)
p1 = baseline
p2 = baseline + effect
pooled_p = (p1 + p2) / 2
effect_size = abs(p2 - p1) / np.sqrt(pooled_p * (1 - pooled_p))
analysis = NormalIndPower()
n = analysis.solve_power(effect_size=effect_size, alpha=alpha, power=power)
print(f"Required per group: {int(np.ceil(n)):,}")
print(f"Total users needed: {int(np.ceil(n)) * 2:,}")
# If daily traffic is 500 users and 50% go to each group:
daily_per_group = 250
days_needed = int(np.ceil(n)) / daily_per_group
print(f"Test duration: {days_needed:.0f} days")
Additional considerations: - Run for a minimum of 1-2 full weeks to capture day-of-week effects - Don't peek at results and stop early (inflates false positives) - Pre-register the hypothesis and analysis plan before running - Ensure proper randomisation (users, not sessions, if possible)
[Senior] You run 20 A/B tests per month and 15% of them come back as significant (p < 0.05). Should you be confident in these results?
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No — this is the multiple testing problem. If you run 20 tests with α = 0.05, you'd expect 1 false positive by chance alone (20 × 0.05 = 1), even if none of the treatments have a real effect.
15% significant out of 20 tests = 3 significant results. But 1 of those is probably a false positive just from the number of tests run.
Solutions:
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Bonferroni correction: divide α by number of tests. For 20 tests, use α = 0.05/20 = 0.0025 as the significance threshold.
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Benjamini-Hochberg (FDR control): less conservative than Bonferroni, controls the expected proportion of false positives.
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Pre-register hypotheses: only test things you had a strong prior reason to believe would work — this reduces the number of tests and their false positive rate.
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Bayesian A/B testing: use a prior distribution on the effect size rather than null hypothesis significance testing — naturally accounts for multiple comparisons.
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Replication: significant results should be replicated in a follow-up test before full rollout.