Clinical Trials Data Specialist / Director, Clinical Science

Job ID: 17447 | Type: Permanent | Expertise: Clinical Research & BiometricsRecruiter: Kerry Harris (Senior Consultant)Email: kerry@carrotrecruitment.comPhone: +44 (0)2392 316 039Clinical Trials Data Specialist / Director of Clinical ScienceLocation: Hybrid/Remote (London Office Hub – 1 day per week)Working Pattern: Full-Time | PermanentCarrot 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 processEverything you need to know about this roleYou 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 findingsPerforming patient-level data review, including laboratory results, adverse events, concomitant medications and protocol deviationsSupporting medical data review activities, data cleaning and query managementReviewing clinical listings, tables, figures, dashboards and patient narrativesCollaborating with cross-functional teams to support interim analyses, safety reviews and database lock activitiesContributing to protocol amendments, case report forms and other study documentationSupporting safety signal identification and medical interpretation of clinical trial dataMaintaining awareness of therapeutic area developments and emerging clinical evidenceContributing to the delivery of high-quality clinical development programmesExperience and qualities that make you a strong fitDegree 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 terminologyAbility to interpret complex clinical datasets and identify medically relevant trends and safety signalsFamiliarity with EDC systems, clinical data review tools and data visualisation outputsExcellent analytical skills and exceptional attention to detailStrong written and verbal communication skillsComfortable working collaboratively across multidisciplinary teamsProactive, organised and able to manage multiple priorities effectivelyWhat's on offer?Competitive salary and comprehensive benefits package and generous annual bonusHybrid/remote working with the opportunity to attend the London office hub once per weekOpportunity to join an innovative and growing biotechnology organisationWork on cutting-edge oncology clinical development programmes in a collaborative, science-led teamExposure to cross-functional clinical development activitiesApply 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