Clinical Scientist

Orchard Therapeutics - U.S.; London; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading biotechnology gene therapy company in London is seeking a Clinical Scientist to support clinical research projects. The role involves authoring clinical documents, managing study deliverables, and ensuring compliance with regulatory standards. Ideal candidates will have experience in clinical science and possess excellent communication skills. Join a dynamic team dedicated to innovative therapies for rare diseases.

Qualifications

• Experience in protocol writing and clinical trial activities.
• Understanding of GCP/ICH and regulatory environments.

Responsibilities

• Author and update clinical study documents.
• Support clinical study deliverables and monitor trial progress.
• Manage vendors such as CROs and consultants.

Skills

Communication

Problem Solving

Collaboration

Education

Degree in Life Sciences: BSc, MSc, or PhD

Tools

Standard Office Software

Job description

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Location:

London, UK

Reporting to:

Director, Clinical Sciences

Job Summary

Orchard Therapeutics is a global biotechnology gene therapy company dedicated to transforming the lives of people affected by rare diseases through the development of innovative, potentially curative cell and gene therapies. Orchard has its global headquarters in London and its U.S. headquarters in Boston and is a wholly owned subsidiary of Kyowa Kirin, a Japan-based Global Specialty Pharmaceutical Company.

The Clinical Scientist role at Orchard Therapeutics supports the Clinical Sciences leads for various programs and projects. The successful candidate will contribute to project planning, clinical research documentation, and key activities of clinical development. This is a unique opportunity to join an agile, progressive team working on innovative therapies.

The position suits a dynamic, motivated individual with prior clinical science experience, eager to learn and develop skills, and interested in working collaboratively in a fast-paced, high-impact environment.

Key Responsibilities

• Author and update clinical study documents (protocols, regulatory documents, reports, publications).
• Support clinical study deliverables, including updates and regulatory briefing books.
• Assist the Clinical Science team with: review and maintenance of study documents, monitoring trial progress, troubleshooting, regulatory document preparation, data review, and literature research.
• Prepare meeting materials, minutes, and maintain program folders.
• Track project timelines, activities, milestones, and budget.
• Support quality assurance in clinical studies and prepare presentations for scientific meetings.
• Manage vendors such as CROs and consultants.

Requirements

Knowledge and Experience

• Experience in protocol writing, clinical trial activities, and report writing, gained through roles like Clinical Researcher, CRA, CTA, or Clinical Scientist.
• Understanding of GCP/ICH and regulatory environments to ensure compliance and data integrity.
• Experience in rare diseases, gene therapy, pediatrics, neurology, or metabolic fields is preferred.

Skills and Abilities

• Responsible, collaborative, and well-organized.
• Flexible, data-savvy, curious, and problem-solving minded.
• Excellent communication skills in English, both written and verbal.
• Proficient with standard office software.

Education

• Degree in Life Sciences: BSc, MSc, or PhD.

Orchard is an equal opportunity employer committed to diversity and inclusion. Applications are assessed based on qualifications and job requirements, adhering to all applicable legislation and regulatory standards.