Biotechnology Jobs

• Zug, Switzerland
• Hybrid · 2 days in office
• US$266,250 – US$443,750 pa
• Director · manages people

Leads global development of an oncology medicine from clinical proof of concept to approval in first major markets, acting as single point of accountability. Builds and directs a matrixed Medicine Development Team spanning clinical, medical, commercial and manufacturing, driving strategy, governance and go/no-go decisions. Hybrid role with at least two days on-site.

• London
• Hybrid · 2 days in office
• US$266,250 – US$443,750 pa
• Director · manages people

Strategically leads global development of an oncology medicine from clinical Proof of Concept to approval in first major markets, acting as single point of accountability. Builds and leads a matrixed Medicine Development Team spanning clinical, medical, commercial and manufacturing, driving strategy, governance, budgets and lifecycle planning.

• 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.

• Leeds
• Director · manages people

Owns product strategy, roadmap and innovation for clinical pharmacology clinics and bioanalytical labs, spanning early-phase platforms like ClinSpark, LIMS/LIS, ELN, instrument connectivity and lab automation. Builds business cases and secures funding, governs a regulated portfolio, and leads multidisciplinary product teams and vendors across distributed sites.

ClinSpark · LIMS · LIS +7

• Reading
• Senior

Monitors oncology clinical trial sites through selection, initiation, monitoring and close-out visits, ensuring GCP and ICH compliance. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains Trial Master File documentation. Works within a biotech-focused team supporting emerging biopharma sponsors.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• Salt Lake City, United States
• Mid-level
• Contract

Develop, optimize and validate cell-based and biochemical assays for automated high-throughput screening, running workflows at scale across 384- and 1536-well formats. Work in a cross-disciplinary team with biologists, automation and data scientists, documenting methods so assays transfer reliably. A 9-month contractor role, Monday to Friday, 9am-5pm.

Liquid Handlers · Plate Readers · Imagers +5

• London
• Director · manages people

Lead global labelling strategy for assigned products across early and late-stage development, lifecycle management and marketed portfolios, serving as Therapeutic Area Lead. Drive core labelling documents including CCDS, USPI and EU PI, lead health authority negotiations, and shape a future USPI operating model while championing digitalisation and AI-enabled labelling solutions.

FDA · EMA · ICH

• 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…

• London
• Hybrid
• £47,540 – £88,289 pa
• Mid-level

Manage regulatory activities for clinical trial applications across an assigned portfolio, working with study teams, country leads and cross-functional partners. Anticipate regulatory risks, coordinate responses to Health Authority queries and maintain product information in compliance systems, while contributing to automation and simplification initiatives.

• Home Worker
• Remote
• £47,540 – £88,289 pa
• Mid-level

Manages regulatory activities for clinical trial applications across an assigned portfolio, leading high-quality submissions and coordinating responses to Health Authority queries. Works closely with study teams, country leads and cross-functional partners to identify regulatory risks early and secure timely approvals, while contributing to simplification and automation initiatives across Regulatory Affairs.

• 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

• Stevenage
• On-site
• Entry level
• Shift work

Hands-on manufacturing role producing autologous cell therapies, with roughly 85% of time spent in a GMP cleanroom operating cell-processing equipment, completing documentation and supporting environmental monitoring. Two levels are open: an entry-level Associate Operator and an Operator I for those with GMP or cleanroom experience who take on cell culture, sampling and drug product inspection duties.

GMP Cleanroom · Cell-Processing Equipment

• London
• Hybrid · 3 days in office
• Senior

Lead translational pharmacology for an AI-first drug discovery team, shaping neurodegeneration strategy and target validation. Bridge dry-lab predictive models with experimental biology, designing screening cascades and profiling AI-designed molecules. Manage CRO partnerships and serve as scientific lead for portfolio programs.

SPR · TR-FRET · Mass Spectrometry

• Cambridge
• Hybrid · 3 days in office
• Director

Leads three mandates for an infectious disease portfolio: defining end-to-end publication strategy from target selection to clinical development, securing grants and partnerships with NGOs and philanthropic funders, and horizon-scanning emerging biotechnology. Partners with discovery, clinical, data and external academic stakeholders, coaching teams and influencing senior decision-makers.

• Reading
• Remote
• Lead

Provides strategic medical and scientific subject matter expertise in hematology-oncology, advising internal stakeholders on protocol design, clinical development plans and proposals, and supporting client bid-defense meetings. Acts as an internal and external consultant across the research and development lifecycle, coaching project teams and collaborating with business development and operations. Greater independence is expected over time under the therapeutic area head.