Clinical Trials Data Specialist

Clinical Trials Data Specialist / Director of 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