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Senior Biostatistician

Job in 110006, Delhi, Delhi, India
Listing for: Planet Pharma
Contract position
Listed on 2026-03-01
Job specializations:
  • IT/Tech
    Data Security, Data Warehousing, Data Analyst, Data Scientist
Job Description & How to Apply Below
Position: Senior Biostatistician (Contract)
Planet Pharma is urgently seeking a Senior Statistician to work on CONTRACT, remotely in India and to start ASAP.

You will be required to provide immediate support across 4–5 ongoing late‑stage clinical studies. These are active, established programmes requiring hands-on expertise, fast onboarding, and the ability to deliver high‑quality statistical oversight with minimal ramp‑up time.
The successful candidate will play a critical role in supporting key deliverables ahead of an imminent data lock, contributing to analysis planning, SAP updates, interpretation, and collaboration with cross-functional teams.

Key Responsibilities
Provide hands-on statistical support across multiple concurrent late‑stage clinical studies.
Rapidly integrate into active study teams and begin contributing within the first 1–2 days.
Lead and support updates to Statistical Analysis Plans (SAPs) and associated documentation.
Oversee execution of statistical analyses and ensure accuracy, consistency, and compliance with study requirements.
Interpret complex data outputs and communicate insights effectively to cross‑functional stakeholders.
Collaborate closely with clinical, programming, data management, and regulatory teams to ensure study timelines and quality standards are met.
Contribute to ongoing study decisions and strategic planning during a critical period ahead of the data lock.

Must‑Have Experience
Extensive hands-on experience as a Statistician supporting multiple late‑stage clinical trials simultaneously.
Proven ability to operate at pace with minimal onboarding, especially within established studies nearing major milestones.
Strong background in CRO environments, with the ability to navigate complex workflows and deliverables.
Demonstrated expertise in statistical methods for late‑phase clinical research and regulatory‑grade outputs.
Excellent communication skills and the ability to work effectively with cross‑functional teams.

Ideal Candidate Profile
Thrives in fast‑moving, high‑pressure environments and can be relied upon immediately.
Comfortable managing competing priorities across several studies.
Highly analytical with excellent attention to detail.
A proactive problem‑solver who anticipates needs and contributes to strategic decision‑making.
Position Requirements
10+ Years work experience
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