Clinical Trials Data Specialist / Director, Clinical Science

Location: Hybrid/Remote (London Office Hub – 1 day per week)

Working Pattern: Full-Time | Permanent

Carrot Recruitment is proud to be supporting an innovative biotechnology organisation in their search for a Clinical Trials Data Specialist/Director of Clinical Science. This is an exciting opportunity to join a growing clinical development team, playing a key role in the scientific review and interpretation of clinical trial data across cutting-edge programmes.

This role offers the opportunity to work within a highly collaborative, cross-functional environment, contributing to the delivery of high-quality clinical studies while supporting patient safety and data integrity throughout the clinical development process.

Everything you need to know about this role:

• You will support the ongoing medical and scientific review of clinical trial data, helping to identify clinically meaningful trends, ensure data quality and contribute to key clinical development activities.
• Working closely with Clinical Development, Clinical Operations, Biometrics, Medical, Pharmacovigilance and Regulatory teams, you'll play an important role in supporting informed decision-making throughout the lifecycle of clinical studies.
• You'll be involved in:
• Reviewing clinical, safety and efficacy data to identify trends, discrepancies and clinically relevant findings.
• Performing patient-level data review, including laboratory results, adverse events, concomitant medications and protocol deviations.
• Supporting medical data review activities, data cleaning and query management.
• Reviewing clinical listings, tables, figures, dashboards and patient narratives.
• Collaborating with cross-functional teams to support interim analyses, safety reviews and database lock activities.
• Contributing to protocol amendments, case report forms and other study documentation.
• Supporting safety signal identification and medical interpretation of clinical trial data.
• Maintaining awareness of therapeutic area developments and emerging clinical evidence.
• Contributing to the delivery of high-quality clinical development programmes.

Experience and qualities that make you a strong fit:

• Degree in Life Sciences, Medicine, Pharmacy or a related discipline (MSc, PhD, PharmD or MD preferred).
• Experience reviewing clinical trial data within a biotechnology, pharmaceutical or CRO environment - (5 years+ essential).
• Experience within haematological oncology (essential), ideally multiple myeloma (preferred).
• Strong understanding of clinical trial conduct, GCP, protocol requirements and medical terminology.
• Ability to interpret complex clinical datasets and identify medically relevant trends and safety signals.
• Familiarity with EDC systems, clinical data review tools and data visualisation outputs.
• Excellent analytical skills and exceptional attention to detail.
• Strong written and verbal communication skills.
• Comfortable working collaboratively across multidisciplinary teams.
• Proactive, organised and able to manage multiple priorities effectively.

What's on offer?

• Competitive salary and comprehensive benefits package and generous annual bonus.
• Hybrid/remote working with the opportunity to attend the London office hub once per week.
• Opportunity to join an innovative and growing biotechnology organisation.
• Work on cutting-edge oncology clinical development programmes in a collaborative, science-led team.
• Exposure to cross-functional clinical development activities.

Apply today for your experience to be considered. Please note that applicants must have the full right to work in the UK - no sponsorship is available.