Clinical Research Scientist — PoC Strategy & Protocols Lead

Alchemab; Cambridgeshire and Peterborough; On-site; GBP 40,000 - 70,000; Full time

Job summary

A biopharmaceutical company in the UK seeks a Clinical Research Scientist to collaborate on clinical designs and draft key documents for early clinical trials. The ideal candidate will have advanced scientific training, experience in early clinical development, and a strong ability to work with cross-functional teams. Responsibilities include authoring clinical protocols, defining endpoints, and driving KOL discussions. Exceptional communication skills and a solid regulatory understanding are essential for this role. Employment type is full-time.

Qualifications

• Advanced scientific training (PhD, PharmD, MD) or MSc with strong industry experience.
• Solid track record in early clinical development (FIH / Phase 1 / 2).
• Demonstrated authorship of clinical protocols and related study documents.
• Experience with medical data review and study interpretation.
• Strong understanding of biotech product development processes.

Responsibilities

• Participate actively in gap assessments and define clinically meaningful endpoints.
• Draft the Clinical Concept Sheet for CRO selection and review clinical protocols.
• Research and educate on clinical trial strategy and design.

Skills

Laboratory Experience

Machine Learning

Python

AI

Bioinformatics

C / C++

R

Biochemistry

Research Experience

Natural Language Processing

Deep Learning

Molecular Biology

Education

PhD, PharmD, MD or equivalent

MSc with strong industry experience

Job description

A biopharmaceutical company in the UK seeks a Clinical Research Scientist to collaborate on clinical designs and draft key documents for early clinical trials. The ideal candidate will have advanced scientific training, experience in early clinical development, and a strong ability to work with cross-functional teams. Responsibilities include authoring clinical protocols, defining endpoints, and driving KOL discussions. Exceptional communication skills and a solid regulatory understanding are essential for this role. Employment type is full-time.