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Senior Clinical Scientist - single client dedicated

UK, Reading🌐 Remote💼 Full-time🗓 2026-09-03 → 2026-09-26

Core

Design and conduct clinical studies to evaluate the safety and efficacy of innovative treatments, focusing on early clinical development and clinical pharmacology.

Role type

Senior Clinical Scientist (Early Development/Clinical Pharmacology)

Builds

Clinical development plans, protocols, regulatory submissions (IND, IB), and study reports for new medicines.

Domain

Healthcare / Clinical Research / Clinical Pharmacology

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

Clinical study design, protocol authoring and review, safety and efficacy data analysis, regulatory submission preparation, cross-functional collaboration, project timeline and budget management

Preferred skills

Clinical pharmacology, immunology, oncology

Technologies

Clinical trial management systems, statistical software for analysis

Responsibilities

Provide strategic leadership for clinical programs supporting early development; Author/Review/Approve clinical protocols, analysis plans, study reports, and regulatory submissions; Execute Clinical & Clinical Pharmacology studies; Review and summarize clinical safety or efficacy data; Contribute to the development of program strategy and clinical development plans; Ensure adherence to agreed timelines and budgets.

Seniority

Senior, hands-on IC

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