Biotechnology Jobs

• Stevenage
• Hybrid · 2 days in office
• US$202,500 – US$371,250 pa
• Director · manages people

Leads clinical development strategy for hepatology assets within the Respiratory, Immunology & Inflammation Research Unit, identifying next-generation liver disease targets and progressing them to proof-of-concept. Accountable for clinical development plans, study protocols, medical monitoring and safety governance, and chairs the Clinical Matrix Team. Hybrid role with at least two days per week on-site.

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$284,625 – US$474,375 pa
• Director · manages people

Leads clinical development medical activities for cardiovascular programs across early and later phase studies, shaping clinical development plans, study designs and translational strategies. Provides medical monitoring and safety oversight, serves as clinical point of contact with regulators and investigators, and leads a cross-functional clinical matrix team within the Cardiovascular Medicine group. Requires a medical degree, board certification in cardiovascular medicine and at least five years of clinical research experience.

• Reading
• Senior

Monitors clinical trial sites across the UK, handling selection, initiation, monitoring and close-out visits in line with GCP and ICH guidelines. Manages multiple protocols, drives subject recruitment, tracks regulatory submissions and CRF data, and maintains Trial Master File documentation. Based in Reading with regular travel to investigative sites.

• London
• Lead

Lead the development of country, site and patient enrollment strategies for complex global clinical trials, analysing clinical and operational data to shape feasibility and study delivery. Present recommendations to clients and senior stakeholders, with a particular focus on APAC opportunities including China. Mentors colleagues and acts as subject-matter expert for planning tools.

• London
• Remote
• Mid-level

Oversees medical coding activities across clinical studies, managing coding dictionaries such as MedDRA and WHODrug, reviewing coded data for accuracy and compliance, and preparing coding reports for medical review. Acts as subject matter expert, delivering training and partnering with Clinical Development, Pharmacovigilance and Data Management teams to drive process improvements and regulatory compliance.

MedDRA · WHODrug

• London
• Remote
• Senior · manages people

Leads cross-functional clinical trial teams for biotech clients, owning project plans, budgets, P&L, risk management and client relationships from Phase I to III. Requires strong CRO experience and therapeutic expertise in oncology plus areas such as dermatology, women's health, neurology, rare disease or radiopharmaceuticals, working fully remotely within a select EMEA country.

Microsoft Excel · PowerPoint · Microsoft Word +1

• High Wycombe
• Entry level
• Internship

A 12-month industry placement within the Integrated Data Analytics and Reporting function, focused on Clinical and Statistical Programming. The student applies SAS, R, Python, RPA and Power Automate to analyse trial data, build AI-driven tools and automate clinical reporting, while collaborating with programming experts across disease areas.

SAS · R · Python +4

• 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.

• Maidenhead
• Mid-level

Monitors and oversees clinical trial sites across the Midlands, handling site initiation, monitoring visits and closeouts while ensuring GCP compliance and patient safety. Also supports feasibility assessments, investigator recruitment, vendor coordination, SAE reporting and mentoring of junior team members within a global FSP team.

• 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

• United Kingdom
• £55,000 – £70,000 pa

This role involves leading in-vitro toxicology studies within a regulated preclinical environment, focusing on assay development and execution for product safety assessment. The scientist will apply advanced cell-based methods including Neutral Red, Ames, and micronucleus assays, interpret complex biological data, and support regulatory submissions. Collaboration with internal teams and external partners is key, alongside method validation and scientific reporting in a quality-assured laboratory setting.

• United Kingdom
• Remote
• Lead

Leads the design and implementation of bioanalytical strategies for a client-dedicated global biopharma team, ensuring lab-based activities align with context of use. Manages experimental design, tech transfer and regulatory submissions, interacting with lab scientists, cross-functional groups and Health Authorities in a matrix environment.

ddPCR · qPCR · RT-qPCR +6

• 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

• London
• Hybrid
• €63,600 – €118,000 pa
• Lead · manages people

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.

Artificial Intelligence