Biotechnology Jobs

• Poznan Grunwaldzka
• Hybrid
• £410,250 – £683,750 pa
• Director

Provides medical and scientific leadership in safety evaluation and risk management for oncology assets in clinical development, interpreting safety data, escalating signals and delivering evidence-based benefit-risk recommendations. Leads Safety Review Teams and cross-functional matrix groups, representing Safety to governance committees and regulatory authorities. Hybrid role based in the UK, Belgium, Poland or Italy.

• Belgium-Wavre
• Hybrid
• Director

Provides medical and scientific leadership in pharmacovigilance and risk management for oncology assets in clinical development, interpreting safety data, detecting and escalating signals, and delivering evidence-based benefit-risk recommendations. Represents Safety on cross-functional clinical matrix teams and Safety Review Teams, and presents to senior governance committees and regulators. Hybrid role based in the UK, Belgium, Poland or Italy.

• Oxford
• On-site
• Senior

Hands-on role designing, prototyping and characterising novel MEMS devices and sensor interfaces for next-generation nanopore sequencing, taking concepts from proof-of-concept to integrated multi-channel sensing systems. Works closely with a Senior Electronics R&D Engineer and external fabrication partners, tackling microfabrication, materials, device architecture and MEMS-electronics integration while helping establish MEMS engineering capabilities for a growing multidisciplinary team.

Oracle Cloud

• Oxford
• On-site
• Senior

Lead metabolic engineering and synthetic biology work to manipulate plant respiration, energy status and redox balance, first in cell cultures then in whole plants. Use iterative design-build-test-learn cycles with physiological, imaging and multi-omics phenotyping, contributing to IP and commercial translation within a multidisciplinary institute.

• Cambridge, United States
• Hybrid · 3 days in office
• Senior · manages people

Lead in vitro and cellular pharmacology strategy for small-molecule drug design programs, defining screening cascades and guiding biophysical, biochemical and cell-based assays from hit identification to candidate selection. Bridge computational AI/ML predictions with laboratory validation, managing CRO partnerships and collaborating with chemistry, structural biology and translational teams.

SPR · ITC · CRO

• Cambridge, United States
• Hybrid · 3 days in office
• Senior · manages people

Designs and implements translational strategies for small molecule oncology and immunology programs, from early discovery through candidate selection and clinical phase. Oversees CRO activities, PK/PD and safety assessments, and biomarker strategies, bridging computational predictions with laboratory validation. Some roles include managing 2-3 in vivo pharmacologists.

Machine Learning · AlphaFold

• Macclesfield
• On-site
• Permanent

Collects environmental monitoring and cleaning validation samples in sterile manufacturing facilities, then performs microbiological and QC testing such as bioburden, endotoxin, concentration and conductivity analysis. Manages the full sample lifecycle in LIMS, reviews monitoring plans, investigates out-of-specification results and GMP-assesses data. Works a continuous two-week rotating pattern of 11-hour day shifts.

LIMS

• Macclesfield
• On-site
• Senior · manages people
• Permanent

Acts as the key analytical point of contact for clients, leading the transfer of commercial analytical methods across multiple laboratory sites and ensuring their robustness, performance and compliance for drug substances. Coordinates analytical activities, supports change programmes and market access projects, and leads a small team of scientists while working with Quality, Regulatory and Manufacturing. Based at a pharmaceutical client facility in Macclesfield.

• 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.

• United Kingdom
• Remote
• Lead

Lead medical writer dedicated to a single client, authoring and reviewing clinical study reports, protocols, IBs, INDs and MAAs while advising on document strategy and regulatory requirements. Provides senior review, mentoring and training to junior writers and program managers, and leads process improvement initiatives. Therapeutic experience in neurology, immunology, oncology or vaccines is valued.

• 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
• On-site
• Senior

Owns all aspects of hardware design for automated cell-production machines, from concept through to manufacture, improving robustness and reliability. Leads development of systems interfacing with optics and fluidics, refines test rigs and quality processes, and helps shape engineering culture. Based on-site in the lab at Imperial College's White City innovation hub.

Arduino · Raspberry Pi · Adafruit +1

• Manchester
• Mid-level

Conducts site qualification, initiation, monitoring and close-out visits for clinical trials, 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. Embedded in a sponsor-dedicated functional service partnership model.

Investigator Site Files · Trial Master Files

• 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

• London
• Hybrid · 3 days in office
• Director · manages people

Lead national medical strategy for the Respiratory & Immunology business unit, spanning inhaled therapies and biologics. Define pre-launch and launch medical plans, drive NHS transforming-care initiatives, and oversee MSL and healthcare delivery teams. Provide scientific leadership across regulatory, market access and real-world evidence work.

NHS · NICE · SMC +3