Biotechnology Jobs

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$242,250 – US$403,750 pa
• Director · manages people

Owns the clinical strategy, scientific narrative and benefit-risk framework for genitourinary cancer assets, acting as the senior clinical authority on the Medicine Development Team core quad. Sets asset-level evidence-generation and governance direction while Senior Scientists handle study-level delivery, and represents Clinical Development in health authority and external engagements. Hybrid role with at least two on-site days per week.

AI · Advanced Analytics

• Zug, Switzerland
• Hybrid · 2–3 days in office
• US$222,750 – US$371,250 pa
• Director

Serves as the physician within a clinical programme team, leading medical monitoring, safety oversight and data interpretation for GI oncology studies. Partners with a Senior Scientist and cross-functional matrix teams on protocol development, regulatory interactions and investigator engagement. Requires an on-site presence 2-3 days a week across UK, Swiss or US sites.

AI-enabled Insights

• London
• Remote
• Director

Medically responsible at trial level across preparation, conduct and reporting phases, providing medical expertise and oversight from Trial Design Outline to Clinical Trial Report. Dedicated to a single sponsor in the EMEA region, the role involves authoring high-quality clinical trial protocols, co-authoring Clinical Quality Monitoring plans, integrating medically relevant data into risk-based quality management, and performing ongoing reviews of medical data.

• Harrow
• Remote
• Mid-level

Independently leads statistical aspects of low-to-moderate complexity clinical trials, developing complex analysis strategies and executing them with SAS or R. Reviews analysis datasets, quality-controls statistical deliverables, and contributes to trial design, analysis plans, and regulatory submissions. Works within global cross-functional teams, liaising with clients on data analysis, scope, and budget.

SAS · R

• United Kingdom
• Remote
• Entry level

Supports clinical trial site management remotely, liaising with CRAs and study teams on site preparedness, document collection, vendor trackers and remote monitoring tasks. Handles essential documents, site payments, reconciliations and centralized monitoring reviews in line with SOPs and ICH GCP. Suits an early-career life sciences graduate seeking a UK-based remote clinical research role.

EMR · EHR · CTMS +2

• London
• Hybrid
• £67,900 – £126,100 pa
• Senior

Co-leads cross-functional Clinical Trial Teams and global studies from planning through close-out, managing timelines, budgets, risks and inspection readiness. Partners across global and local functions on recruitment, data operations and vendor performance, while championing operational excellence and continuous improvement.

• Home Worker
• Remote
• £67,900 – £126,100 pa
• Lead · manages people

Lead and develop a global regulatory team delivering clinical trial submissions and approvals, combining people leadership with regulatory expertise. Drive process improvement, simplification and automation while building stakeholder partnerships across Regulatory Affairs. Hybrid or remote working within the UK, with occasional office presence in London.

• United Kingdom
• Remote
• Lead · manages people

Leads global regulatory strategy for Phase 1-4 clinical trials, preparing and assembling CTA submissions and acting as the client-facing liaison with sponsors and regulatory agencies. Represents the regulatory department in bid defense and launch meetings, managing project teams and reviewing clinical and scientific documentation.

Microsoft Word · Microsoft Excel · PowerPoint

• Taunton
• On-site
• £49,387 – £56,515 pa
• Lead · manages people
• Permanent

Lead a team of Biomedical Scientists and support staff across Bacteriology, Parasitology, Virology, Molecular and Mycology, rotating through all areas. Responsibilities include training, appraisals, quality management, policy development, clinical trials and senior management on-call, with lone working on evening and weekend shifts.

LIMS · Q-Pulse · Kiestra

• Maidenhead
• Lead · manages people

Client-facing biostatistics role leading design and analysis of non-interventional and low-interventional studies using real-world data such as claims, EHR and registries. Applies causal inference methods, target trial emulation and synthetic control arms, authors SAPs and manages SAS programming teams, while supporting proposals, budgeting and bid defences.

SAS · CDISC

• United Kingdom - Walton Oaks
• Hybrid

Lead and implement regional regulatory strategies for assigned products, acting as the regional representative within Pfizer's Global Regulatory Strategic Team. Accountable for timely submissions, approvals and optimal interactions with Health Authorities, partnering cross-functionally to align regulatory plans with commercial goals.

ChatGPT · Microsoft Copilot

• Ireland
• On-site
• Mid-level · manages people
• Permanent

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

• London
• Lead · manages people

Provides technical leadership in setting up and operating a CDMO site, leading process development and analytical method development projects for cell therapy manufacture. Plans technology transfers, ensures regulatory compliance, drives continuous improvement, and mentors colleagues while engaging directly with clients.

MHRA · EMA · FDA

• 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

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.