Biotechnology Jobs

• Manchester
• On-site
• Entry level

Perform complex clinical procedures such as ECG, phlebotomy, spirometry, cannulation and cardiac telemetry on trial volunteers, and collect and report data per protocol. Support Phase I-IV studies at a hospital-based research facility, ensuring compliance with GCP and SOPs while orienting volunteers and assisting nursing colleagues.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• London
• Hybrid
• Lead · manages people

Serves as the clinical trial pharmacy subject matter expert across global oncology programmes, advising on investigational product handling, preparation, storage and accountability, and on hazardous drug and CSTD requirements. Develops pharmacy manuals and training for site pharmacists and study teams, supports audits and CAPAs, and oversees FSP pharmacists and external vendors. Hybrid role spanning London, Paris or Cambridge MA.

Closed System Transfer Devices

• Leeds
• On-site
• Senior

Lead early-phase clinical trials as Principal Investigator or Project Physician, taking studies from start-up through closeout and the Clinical Study Report. Work across first-in-human studies, multiple therapeutic areas and an NHS Trust collaboration, with on-call cover and mentoring of less experienced physicians.

MHRA · cGMP · NHS Trust

• London
• £47,500 pa
• Entry level
• Contract

Lead an independent research project on eukaryotic cell cycle regulation in the fission yeast model, using cell biology, molecular genetics and biochemistry to study how CDK activity coordinates DNA replication, mitosis and division. The role sits in a collaborative lab and includes scope to develop new approaches and help support PhD students.

Schizosaccharomyces pombe

• London
• Remote
• Senior

Lead monitoring activities for assigned oncology clinical trial sites, from site activation through closeout, conducting both onsite and remote visits, source data verification and regulatory document oversight. Partner with a dedicated sponsor in an FSP model, driving enrollment, resolving protocol deviations and supporting audit readiness. Requires at least five years of oncology clinical research experience and up to 75% travel.

CTMS · EDC

• Saffron Walden
• Hybrid · 1–2 days in office
• Senior
• Temporary

Combines hands-on development of production bioinformatics services like Job Dispatcher with scientific and technical leadership, shaping product strategy, roadmaps and backlog priorities. Works with scientists, engineers and infrastructure teams on HPC, Nextflow, SLURM and containerised tools, and represents services in committee meetings.

Job Dispatcher · FiRE · Angular +7

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

A postdoctoral research associate role delivering the insect-focused laboratory components of a consortium project on a planthopper-vectored bacterial plant disease. The postholder investigates vector ecology and transmission biology using insect rearing, bioassays, EPG analysis and molecular techniques such as PCR and qRT-PCR, with occasional travel within the UK and Europe.

Electrical Penetration Graph · Bioinformatics

• Saffron Walden
• Hybrid · 2 days in office
• £3,452 pm
• Mid-level
• Contract

Maintains microbial genomes in Ensembl, loading new annotations, coordinating releases and diagnosing data issues. Develops functional annotation and pangenome pipelines, evaluates taxon-specific annotation tools, and builds Nextflow or Snakemake workflows with Python, relational databases and HPC or cloud infrastructure.

Nextflow · Snakemake · MySQL +7

• Cambridge
• Senior
• Permanent

Lead biophysical binding characterisation, predominantly using Surface Plasmon Resonance, to interrogate Bicycle® molecules and triage screening cascades. Design and optimise bespoke assays, explore orthogonal technologies such as Carterra, AlphaScreen and mass photometry, and partner with computational and structural biology teams on structure-based drug design. Mentors junior colleagues within the Platform Technology group.

SPR · Carterra · AlphaScreen +4

• Reading
• Mid-level

Conducts site qualification, initiation, monitoring and close-out visits for a pharmaceutical sponsor as an embedded member of IQVIA's Clinical Functional Service Partnership team. Monitors patient safety, data integrity and protocol compliance, mentors junior staff, and travels up to 40-60% of the time within the region.

Investigator Site Files (ISF) · Trial Master Files (TMF)

• Leeds
• Hybrid
• Senior
• Permanent

On-site CRA role monitoring Phase I–Ib studies inside a 100-bed Leeds Clinical Research Unit, covering pre-study, initiation, routine monitoring and close-out visits. Works alongside clinic, pharmacy and lab teams during first-in-human dosing days, using integrated eSource and EDC systems to focus on data integrity and protocol compliance rather than mechanical SDV.

eSource · EDC

• United Kingdom
• Remote
• Senior

Monitors investigator sites using a risk-based approach, conducting remote and on-site visits to assess protocol and regulatory compliance, performing SDR, SDV and CRF review, and documenting findings in reports. Acts as a site processes specialist ensuring trials follow ICH-GCP, applicable regulations and SOPs, while developing collaborative relationships with investigational sites and supporting audit readiness.

CTMS · Microsoft Office

• 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
• Lead

Ensures clinical trials comply with quality standards, SOPs and health authority regulations, partnering with site management and therapeutic area leads. Builds cluster quality plans, leads CAPA and root cause investigations, and supports audit and inspection readiness across internal and FSP teams. Also handles local regulatory intelligence and supplier quality assessments.

Quality Risk Management System

• High Wycombe
• Hybrid · 3 days in office
• Entry level
• Internship

A 12-week summer internship in EMEA Global Regulatory Affairs within the Oncology therapeutic area, working on a hybrid model with three days on site. Interns join a global matrixed team supporting clinical strategies and Phase I-III oncology studies, contributing to regulatory strategy, clinical trial applications and product registration activities, with a mentor, cross-functional team meetings and a research poster presented at a company-wide symposium.

Microsoft Outlook · Microsoft Excel · Microsoft PowerPoint +5