Clinical Scientist

JR United Kingdom; Warrington; Remote; GBP 40,000 - 60,000; Full time

Job summary

A leading biotechnology company in Warrington is seeking a Clinical Scientist to support clinical trial design and execution. The ideal candidate will have an advanced life sciences degree and 2-6+ years in clinical development. Responsibilities include designing clinical protocols, contributing to study documents, and collaborating with CROs and clinical sites. This position will entail remote work with travel as needed.

Qualifications

• 2–6+ years in clinical development or operations.
• Knowledge of ICH GCP and trial methodology.
• Experience in rare diseases and clinical site management is preferred.

Responsibilities

• Design and develop clinical study protocols and amendments.
• Contribute to study documents like IBs, consent forms, CRFs.
• Support trial conduct with scientific input.

Skills

Strong communication

Multitasking

Education

Advanced degree in life sciences or health discipline (PhD, PharmD, MD, or MS)

Job description

Social network you want to login/join with:

Clinical Scientist, Warrington, Cheshire

Client: AIRNA

Location: Warrington, Cheshire, UK (Remote position with travel)

Job Category: Other

EU work permit required: Yes

Job Views: 1

Posted: 22.08.2025

Expiry Date: 06.10.2025

Job Description:

COMPANY OVERVIEW

AIRNA is a biotechnology company focused on RNA editing, developing therapies for various diseases. Our platform is based on groundbreaking research and aims to provide functional cures by repairing or introducing genetic variants.

We have raised $245 million from top investors and value teamwork, resilience, and excellence. Our teams are based in Cambridge, MA, and Tübingen, Germany.

JOB OVERVIEW

The Clinical Scientist supports clinical trial design, execution, and analysis within AIRNA’s RNA editing platform, ensuring scientific integrity and operational excellence.

RESPONSIBILITIES

• Design and develop clinical study protocols and amendments
• Contribute to study documents like IBs, consent forms, CRFs, recruitment materials
• Support trial conduct with scientific input
• Monitor data quality and safety signals
• Collaborate with CROs, sites, and internal teams to resolve issues
• Build relationships with clinical sites and staff
• Review and interpret clinical data
• Assist in regulatory documentation and reports
• Work with cross-functional teams and present findings

QUALIFICATIONS

• Advanced degree in life sciences or health discipline (PhD, PharmD, MD, or MS)
• 2–6+ years in clinical development or operations
• Knowledge of ICH GCP and trial methodology
• Strong communication and multitasking skills
• Experience in rare diseases and clinical site management is preferred