517 jobs for “Research Associate In Biomaterials And I”
IQVIA
Conducts site qualification, initiation, monitoring and close-out visits for a dedicated clinical trial program, ensuring GCP compliance, patient safety and data integrity. Builds relationships with investigators, resolves data queries, mentors junior staff and travels up to 40-60% within the region.
Investigator Site Files · Trial Master Files
IQVIA
Monitors clinical trial sites across selection, initiation, monitoring and close-out visits, ensuring compliance with GCP and ICH guidelines. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains Trial Master File documentation. Works within a sponsor-dedicated team, liaising with sites and study team members.
Leads the full statistical contribution to a clinical development programme, defining statistical strategy for trial design, analysis and regulatory submissions, and representing Biostatistics in interactions with the FDA, EMA and PMDA. Also manages outsourcing to CROs and internal statistical programmers, and supports departmental improvement initiatives.
SAS · R
Acts as the operational 'COO' of a drug or vaccine asset, owning the single integrated project plan and partnering with project leads to steer strategy through complexity. Drives critical-path acceleration, risk management, governance preparation and cross-functional handoffs, with budget and resource forecasting using tools such as Planisware or MS Project.
Planisware · MS Project
Relation Therapeutics
Lead the team behind hybrid on-prem and cloud compute infrastructure, Kubernetes clusters, and scientific compute environments supporting ML and drug discovery. Own platform strategy, CI/CD maturity, observability, and security controls for sensitive patient-derived data, reporting to the VP of Engineering.
Kubernetes · Kubeflow · GPU Compute +3
Acts as the primary interface between business stakeholders, biostatisticians, statistical programmers and technical delivery teams, translating clinical and statistical requirements into scalable R-based analytics, automation workflows and enterprise reporting. Leads requirement workshops, manages a small team, and oversees releases with end-to-end traceability, regulatory compliance and audit readiness across the clinical trial lifecycle.
Provides scientific and medical expertise at study level across early- and late-phase hepatology assets, serving as medical monitor for Phase 1–4 trials and leading protocol, IB, ICF and CSR authoring. Works within cross-functional global study teams and the Clinical Matrix Team, integrating efficacy, safety and biomarker data to inform asset and portfolio decisions, with informal coaching of less experienced clinical scientists.
Acts as the primary interface between business stakeholders, biostatisticians, statistical programmers and technical delivery teams, translating clinical and statistical requirements into scalable R-based analytics, automation workflows and enterprise reporting. Leads requirement workshops, manages a small team and oversees releases with end-to-end traceability, regulatory compliance and audit readiness across development, validation and deployment.
Helical
Hands-on business development role researching pharma and biotech accounts, writing outreach, and owning CRM pipeline hygiene in HubSpot. Works directly with founders and the head of sales, building sales materials and AI workflows while coordinating with the science team ahead of customer meetings.
HubSpot · LinkedIn
Moderna · 1001–5000 people · Late stage
Perform routine cGMP Quality Control testing using HPLC, UPLC, GC, UV spectroscopy, DLS and Karl Fischer analysis, supporting raw materials, in-process materials, drug substance, product release and stability programs. Coordinate and execute global GMP stability studies, manage sample lifecycles in LabVantage LIMS, trend data statistically, and author protocols and regulatory documentation. The role is 100% onsite at the Harwell facility and involves collaboration with manufacturing, QA, regulatory and external testing partners.
LabVantage · LIMS · Generative AI
Moderna · 1001–5000 people · Late stage
Shapes and executes a UK-wide government affairs strategy as a sole contributor, focusing on respiratory vaccines and building relationships across government, Parliament and industry. Involves legislative and regulatory analysis, trade association management, and exploring Generative AI for policy intelligence, working with Communications, Medical and Market Access teams.
Generative AI
AstraZeneca · 10000+ people · Public
Lead UK direct tax compliance and group tax reporting for a FTSE 100 biopharmaceutical business, preparing and reviewing corporation tax computations, patent box and capital allowance claims, and quarterly and year-end tax provisions under Sarbanes-Oxley. Handle HMRC audit queries and negotiations, advise the UK business on legislation changes, and drive process efficiencies through automation and AI.
AI
AstraZeneca · 10000+ people · Public
Lead UK direct tax compliance and reporting for a FTSE 100 biopharmaceutical group, preparing and reviewing corporation tax computations, patent box and capital allowance claims, and quarterly and year-end tax provisions. Advise the UK business on legislation changes, HMRC audits and governance regimes, while driving process efficiencies through automation and AI.
Ellison Institute of Technology · 501–1000 people · Non-profit
Leads the end-to-end event delivery workflow for gene edited and transgenic crops, from transformation output through sampling, molecular confirmation, QC review and handover. Designs and validates genotyping assays (PCR, qPCR, ddPCR, KASP, NGS) and builds stage-gate criteria, LIMS-enabled tracking and vendor strategies across corn and wheat programmes.
Endpoint PCR · qPCR · ddPCR +6
Thermo Fisher Scientific
Monitors investigator sites using a risk-based approach, conducting remote and on-site visits to assess protocol and regulatory compliance, performing SDR, SDV and CRF review, and documenting findings in reports. Acts as a site processes specialist ensuring trials follow ICH-GCP, applicable regulations and SOPs, while developing collaborative relationships with investigational sites and supporting audit readiness.
CTMS · Microsoft Office
