539 jobs for “Research Scientist”
GSK London US$222,750 – US$371,250 pa
Serves as the physician within a clinical programme team, leading medical monitoring and safety oversight for oncology studies and interpreting clinical and safety data. Partners with the Senior Scientist and cross-functional teams on protocol development, regulatory interactions and investigator engagement, with a focus on GI oncology. Requires an on-site office presence two to three days a week.
GSK Waltham, United States US$222,750 – US$371,250 pa
Serves as the physician on a clinical programme team, leading medical monitoring and safety oversight for GI oncology studies. Interprets clinical and safety data, contributes to protocol development, and engages investigators and regulators. Works within a Clinical Matrix Team alongside Clinical Operations, Biostatistics, Regulatory and Pharmacovigilance, with on-site presence 2-3 days a week.
Fortrea Maidenhead
Lead and manage clinical trial sites across a diverse portfolio spanning oncology, neuroscience, cell & gene and CAR-T therapies. The role emphasises patient safety, data integrity and building trusted relationships with investigators, with autonomy and support for complex, innovative study designs.
Fortrea Maidenhead
Monitors clinical trial sites across a diverse portfolio spanning oncology, neuroscience, general medicine, cell & gene and CAR-T therapy. Leads site management, builds relationships with investigators and study teams, and safeguards patient safety and data integrity on complex, first-in-class studies. Distinct for its breadth across therapeutic areas and advanced therapy exposure rather than a narrow single-indication focus.
IQVIA Reading
Leads end-to-end delivery of regional and global clinical trials embedded within a sponsor's team, managing timelines, budgets, risk and cross-functional groups. Also supports bid defence presentations, vendor management and financial forecasting, mentoring less experienced project team members.
IQVIA Reading
Conducts site qualification, initiation, monitoring and close-out visits for a dedicated sponsor program, ensuring GCP compliance, patient safety and data integrity. Builds investigator relationships, resolves queries, maintains inspection-ready documentation and mentors junior team members, with up to 40-60% regional travel.
Parexel Harrow
Drives strategic impact by developing operational and technical solutions for Early Phase clinical trials, collaborating with Enterprise Accounts, Growth Accounts, Commercial Operations and Strategic Business Units. Contributes to business development from opportunity identification through solution design, bid strategy and client engagement, crafting differentiated value propositions and proposal content. Requires 3-5 years of Early Phase Clinical Trials experience and up to 30% travel.
Ipsen London
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.
Danaher Portsmouth
Responsible for new product development and improvement projects for hardware and disposable devices used in the biotech industry, taking initiatives from spec definition through design, testing and validation to manufacturing transfer. Provides technical leadership on complex engineering challenges, applies 3D CAD design, manages project plans and resources, and reports progress to leadership. On-site role with up to 20% international travel.
Parexel London
Leads the success of assigned Functional Service Provider clinical operations programs, covering service delivery, financial performance, resource optimization and regulatory compliance. Provides strategic direction to FSP management teams, builds scalable delivery frameworks and performance metrics, and partners with functional and regional leaders to expand service offerings and grow client relationships.
Ipsen London
Ensures clinical trials comply with quality standards, SOPs and health authority regulations, partnering with site management and therapeutic area leads. Builds cluster quality plans, leads CAPA and root cause investigations, and supports audit and inspection readiness across internal and FSP teams. Also handles local regulatory intelligence and supplier quality assessments.
SPD Development Company Ltd Bedford
Provides statistical expertise across R&D, Clinical, Product Support and Marketing, supporting study design, analysis plans and interpretation of data throughout the product lifecycle. Works as one of three Statisticians in the Statistical & Data Services Team, advising project teams, evaluating product algorithms and communicating findings to technical and non-technical audiences.
Taylorollinson Burgess Hill £35,000 – £40,000 pa
Owns inventory control for a biospecimen provider, setting up processes to keep correct stock levels at redistribution centres in Burgess Hill and one European venue. Covers demand planning, forecasting, reporting to stakeholders and working with Salesforce and Sage X3 across warehouse, logistics and sales teams.
Novartis London €63,600 – €118,000 pa
Lead and develop a team of Central Monitors while shaping risk-based monitoring strategies across a global clinical development portfolio. Oversee trial-data surveillance, signal detection and Key Risk Indicators, translating complex risk signals into actionable insights for Clinical Trial Teams. Works in a global matrix with clinical, data and risk-surveillance teams, driving continuous improvement through analytics and technology.
Novartis Dublin, Ireland €63,600 – €118,000 pa
Lead and develop a team of Central Monitors while shaping risk-based monitoring strategies across a global clinical development portfolio. Oversee trial-data surveillance, signal detection and insight generation, translating complex risk signals into actionable insights and designing study-specific Key Risk Indicators and Quality Tolerance Limits.
