Contract Junior Clinical Scientist – Gene Therapy

Contract Junior Clinical Scientist – Gene Therapy

Location: London, UK (Hybrid – minimum 2 days onsite per week)

Contract: Initial 6-month contract, with rolling extensions

Contract Type: Inside IR35

Start Date: ASAP

Industry: Biotechnology / Gene Therapy / Clinical Development

About the Opportunity

APX Life Sciences is partnering with an innovative, growing gene therapy biotechnology company based in London to recruit a Junior Clinical Scientist on an initial 6-month contract, with the potential for extensions and permanent employment.

This is an excellent opportunity for an early-career professional with approximately 1–2 years of experience within the pharmaceutical, biotechnology or clinical research industry to develop their career in clinical development.

Working alongside an established and highly experienced scientific team, the successful candidate will gain valuable exposure to clinical development activities, scientific documentation, clinical data interpretation and the progression of innovative therapies for patients with rare diseases.

The position would suit an enthusiastic, scientifically minded individual who is keen to take on responsibility, develop their technical knowledge and contribute to meaningful clinical research within a collaborative biotechnology environment.

Key Responsibilities

• Support the preparation, review and maintenance of clinical and scientific study documentation, including Investigator's Brochures (IBs), clinical protocols and other study-related materials.
• Assist with the review of Statistical Analysis Plans (SAPs), Tables, Figures and Listings (TFLs), ensuring consistency between planned analyses and reported clinical outputs.
• Review clinical study documents, support scientific queries and assist with the preparation of scientific correspondence.
• Conduct scientific literature reviews, identify relevant publications and references, and support competitive intelligence activities.
• Prepare regular scientific summaries and research updates to support ongoing clinical development programmes.
• Assist with clinical study transition activities, including the transfer and coordination of study documentation.
• Support cross-functional project activities, including meeting coordination, preparation of minutes, maintenance of timelines, trackers and action logs.
• Work closely with senior Clinical Scientists and cross-functional stakeholders to support the effective delivery of clinical development activities.
• Candidate Requirements

Essential:

• Approximately 1–2 years of relevant industry experience within pharmaceutical, biotechnology, clinical research or a related environment.
• A BSc or MSc in Life Sciences, Biomedical Sciences, Pharmacology, Biotechnology or another relevant scientific discipline.
• Experience supporting clinical trial documentation, scientific research or clinical development activities.
• A good understanding of clinical trial processes, scientific documentation and clinical research principles.
• Strong scientific writing, literature review and analytical skills.
• Excellent organisational skills, attention to detail and the ability to manage multiple activities simultaneously.
• Confident communication and interpersonal skills, with the ability to engage effectively with senior scientific colleagues and cross-functional teams.
• A proactive, adaptable and collaborative approach, with a genuine enthusiasm for learning and professional development.
• Ability to work onsite in London a minimum of two days per week.

Desirable:

• Previous exposure to Investigator's Brochures, clinical protocols, SAPs, TFLs or Clinical Study Reports (CSRs).
• Experience within gene therapy, cell therapy, rare diseases or other specialist therapeutic areas.
• Previous experience working within a sponsor-side clinical development environment.
• Familiarity with clinical data interpretation, scientific publications or regulatory documentation.

Why Consider This Opportunity?

• Gain exposure to innovative gene therapy programmes addressing serious rare diseases.
• Work alongside an experienced team of Clinical Scientists and clinical development professionals.
• Develop hands-on experience across scientific documentation, clinical data review and clinical development activities.
• Join a collaborative, growing biotechnology organisation offering excellent opportunities for professional development.
• Initial 6-month contract with potential for rolling extensions and future permanent employment.
• Hybrid working arrangement, with a minimum of two days per week in London.

How to Apply

Please apply with an updated CV or contact Jack O'Neill at APX Life Sciences directly for a confidential discussion.

Email: jack@apxls.com

Applications from individuals with transferable clinical research or scientific experience are welcomed.