652 jobs for “Data Innovation”
Labcorp
Supports a necropsy laboratory through stock control, reagent preparation, labelling and archiving of animal samples in line with study paperwork and SOPs. Involves general housekeeping, possible assistance with postmortems and foetal sectioning, all within a GLP environment. Training is provided, making it a route into the industry.
Excel · Word
Labcorp
Coordinate genetic toxicology studies alongside Study Directors, handling day-to-day study tasks, drafting protocols and amendments, scheduling sample shipments, and preparing study reports. Requires GLP knowledge and technical writing within a scientific setting, managing multiple changing priorities in an office-based team.
Designs disease data information models for priority discovery areas, writing mapping rules to harmonise biomedical data and building quality checks that keep models trustworthy. Works hands-on in code and modelling tools, using AI assistants daily, and partners with research, ontology and data platform teams to get models adopted.
NCI Thesaurus · MONDO · EFO +6
Designs disease data information models for priority discovery areas, writing mapping rules to harmonise biomedical data and building quality checks to keep it trustworthy. Works hands-on in code and modelling tools, using AI assistants daily, and partners with research, ontology and data platform teams plus external partners.
NCI Thesaurus · MONDO · EFO +6
Ipsen
Leads global clinical data transparency and disclosure across registries and regulatory platforms such as CTIS, EMA Policy 0070 and Health Canada PRCI, acting as subject matter expert for assigned therapeutic areas. Manages vendor partnerships, FOI access requests, redaction and lay summary work, plus SOP governance, compliance reporting and audit readiness within Global Regulatory Affairs Excellence.
CTIS · ClinicalTrials.gov · EU Clinical Trial Register +3
University of Surrey · 1001–5000 people
Develop an independent, externally funded research programme as a Principal Investigator, applying AI and data science to human, animal and environmental health data within a One Health framework. Collaborate across medicine, veterinary science, computer science and engineering, secure UKRI/NIHR/Wellcome funding, publish high-impact work, and teach AI and data science at undergraduate and postgraduate level.
Bristol Myers Squibb
An individual contributor role conducting non-interventional real-world data research for medical and HEOR teams across international markets. You will identify data sources, oversee statistical programming in R, and interpret and present findings to stakeholders. The position requires deep expertise in observational data analysis and offers hybrid working from Uxbridge.
R · GitHub · Claude +2
IQVIA
Conducts site monitoring visits including selection, initiation, monitoring and close-out, ensuring compliance with GCP and ICH guidelines. Manages site recruitment plans, protocol training, regulatory submissions and data query resolution, maintaining Trial Master File documentation. Focused on oncology studies within a biotech-focused clinical research team.
Microsoft Word · Microsoft Excel · Microsoft PowerPoint
IQVIA
Monitors oncology clinical trial sites through selection, initiation, monitoring and close-out visits, ensuring GCP and ICH compliance. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains Trial Master File documentation. Works within a biotech-focused team supporting emerging biopharma sponsors.
Microsoft Word · Microsoft Excel · Microsoft PowerPoint
Mackie Myers
Lead complex formulation development programmes for biologics, acting as subject matter expert and providing technical oversight across multiple client projects. Design experimental strategies, present findings to clients and external stakeholders, and mentor junior scientists within a multidisciplinary team.
Randox Health
Manages the people, resources and performance of a 4-on-4-off laboratory shift, owning KPIs such as productivity, error rates, QC pass rate, instrument downtime and sample backlog. Acts as incident lead and primary escalation point for Shift Leads, coordinating with Clinics, Customer Support, IT and Quality to keep testing accurate and within turnaround time.
Microsoft Word · Microsoft Outlook · Microsoft Excel +2
Owns quality oversight of external CROs, laboratories and test facilities supporting nonclinical and GLP activities, running the full vendor lifecycle from due diligence and quality agreements to risk-based monitoring, CAPAs and governance forums. Coordinates inspection readiness and audit support, ensures compliance with GLP/GCP/GMP, OECD GLP, 21 CFR Part 58 and ALCOA+ data integrity, and leads vendor risk assessments such as FMEA and risk registers.
OECD GLP · 21 CFR Part 58 · Annex 11 +3
Owns quality oversight of external CROs, laboratories and test facilities supporting nonclinical and GLP activities, running the vendor lifecycle from due diligence and quality agreements to risk-based monitoring, CAPAs and inspection readiness. Ensures adherence to GLP/GCP/GMP, OECD GLP, 21 CFR Part 58 and data integrity (ALCOA+), partnering with Nonclinical Development, Procurement, Legal and IT.
OECD GLP · 21 CFR Part 58 · Annex 11 +3
LGC
Hands-on role independently developing, optimising and validating analytical methods using LC-MS, troubleshooting complex analytical challenges and building new testing solutions for specialist laboratories. You own method development projects from feasibility through validation and implementation, working across the business in a busy commercial testing environment under ISO 17025.
LC-MS · GC-MS/MS · HRAM
Thermo Fisher Scientific
Accountable for delivering clean clinical data on complex internal medicine trials within contract timelines, managing operational and quality aspects in compliance with ICH GCP. Leads clinical teams, develops monitoring tools and Trial Master File documentation, and may take on Lead CTM or Clinical Study Manager duties across therapeutic areas.
Outlook · Excel · Word
