Biotechnology Jobs

• London
• Hybrid
• PLN 318,000 – PLN 530,000 pa
• Director

Supports patient safety worldwide by leading signal detection, safety evaluation and risk management for products in clinical development and post-marketing. Prepares global regulatory reports and risk management plans, supports safety governance meetings, and contributes to risk-reduction strategies across cross-functional matrix teams.

Safety Databases · Data Visualisation Tools

• Warsaw, Poland
• Hybrid
• PLN 318,000 – PLN 530,000 pa
• Director

Leads signal detection and evaluation for assigned products, prepares global regulatory reports and risk management plans, and supports safety governance meetings across clinical and post-marketing settings. Works in cross-functional matrix teams, contributes to risk-reduction strategies, and mentors colleagues while driving process improvements in pharmacovigilance.

Safety Databases · Data Visualisation Tools

• Bath
• Mid-level

Conducts site qualification, initiation, monitoring and close-out visits for a CRO embedded within pharmaceutical sponsor teams, ensuring GCP compliance, patient safety and data integrity. Manages site relationships, recruitment strategies, TMF/ISF documentation and risk escalation, with mentoring of junior staff and up to 40-60% regional travel.

Investigator Site Files · Trial Master Files

• Livingston
• Mid-level

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

• Oxford
• On-site
• Senior · manages people

Lead development, qualification, validation and execution of complex cell-based immunoassays generating clinical trial data across therapeutic areas. Act as scientific point of contact within the Immuno-assays group, performing GCP/GLP-compliant sample testing, authoring validation reports, and mentoring junior lab staff. Fully onsite at Harwell, reporting to the Associate Director, Immuno-assay UK.

GraphPad Prism · Microsoft Word · Microsoft Excel +2

• Uxbridge
• Hybrid
• Director

Serves as scientific authority for clinical studies across an assigned asset or indication, from protocol development through CSR review and regulatory submission. Leads clinical oversight of study data with Data Management and Programming, may act as Trial Lead on complex global studies, and presents to investigators, KOLs and senior leadership. Also supports process improvement, training and mentoring within the Clinical Capabilities function.

• Maidenhead
• Mid-level

Unblinded monitoring of pharmacies at clinical trial sites across Scotland and the North of England, with possible additional UK and Ireland sites. Involves Investigational Product oversight, ICH-GCP compliance, eTMF documentation and acting as primary contact for pharmacy monitoring, within a sponsor-dedicated team.

eTMF

• Leeds
• Hybrid · 3 days in office
• Entry level
• Permanent

Develops protocols and clinical study reports for early-phase trials (I-IIa), focusing on safety and pharmacokinetics. Coordinates cross-functional teams and client stakeholders to drive documents from draft to final deliverable, with on-the-job training in medical writing.

• Sheffield
• £39,560 – £48,337 pa
• Entry level
• Contract

Lead the design, assembly and clinical validation of a novel dialyser prototype within the Thermofluids Group, testing with blood-mimicking fluids and human blood to assess cleaning efficiency, clotting risk and biocompatibility. Work alongside two other Research Associates covering numerical simulation and experimental fluid dynamics, in collaboration with the Medical School and Sheffield Teaching Hospitals.

• Ireland

Regional Laboratory Manager – DublinRandox are a world leader in diagnostics for clinical healthcare, toxicology, and food security. Our expertise and product portfolio have assisted laboratories across the world in improving health and saving lives. Our global success is a…

• Belfast
• £50,000 – £60,000 pa
• Lead · manages people

Leads a Clinical Method Development and Validation team, overseeing bioanalytical method delivery for a New Product Development programme. Provides technical leadership in a GLP-compliant lab, acting as expert in extraction techniques and optimising HPLC, UPLC and LCMSMS systems while mentoring the team.

HPLC · UPLC · LCMSMS +1

• United Kingdom
• Remote
• Senior

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

• Stevenage
• On-site
• Mid-level

Performs complex sample preparation and quantitative analysis of small molecules and biotherapeutics using instrumentation such as GC-MS, ICP-OES, HPLC and LC-MS, supporting both GMP and non-GMP stability studies. Works largely independently to set up, maintain and troubleshoot analytical instrumentation, interpret data for technical validity and compliance, and report results to client teams. Based full-time onsite at a pharmaceutical client site as part of a functional service provider partnership.

GC-MS · ICP-OES · HPLC +2

• Maidenhead
• Hybrid · 3 days in office
• US$212,000 – US$251,000 pa
• Director

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/FSPs and contributes to governance and development-plan decisions across therapeutic areas.

SAS · R

• Breda, Netherlands
• Hybrid · 3 days in office
• US$212,000 – US$251,000 pa
• Director

Leads the full scope of statistical contribution to a clinical development programme, defining statistical strategy and methodologies for trial design, analysis and regulatory submissions. Represents Biostatistics in interactions with authorities such as FDA, EMA and PMDA, and manages outsourcing or internal statistical programmers. Two positions support multiple therapeutic areas.

SAS · R