Biotechnology Jobs

• Waltham, United States
• Hybrid · 2 days in office
• US$222,750 – US$371,250 pa
• Director

Provides clinical and scientific leadership across respiratory and immunology clinical development programmes, shaping clinical development plans, study designs and regulatory documents. Leads a cross-functional Clinical Matrix Team, oversees medical monitoring and safety governance, and acts as the clinical point of contact for regulators, investigators and key external experts. Hybrid working with at least two days per week on-site.

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

Provides clinical and scientific leadership across early and late-stage respiratory programmes, shaping clinical development plans, study designs and regulatory documents. Leads a cross-functional Clinical Matrix Team, oversees medical monitoring and safety governance, and partners with biology, regulatory, commercial and statistics groups to advance differentiated medicines.

• Reading
• Senior

Embedded with a global pharmaceutical sponsor, you own end-to-end clinical supply strategy across complex trials: protocol interpretation, label text, demand forecasting, packaging, IRT setup, distribution and temperature-excursion management. You lead vendor oversight, risk assessments and budget tracking while advising study teams and client leadership.

IRT · RTSM · ERP +3

• 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.

• 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
• Lead

Lead the safety assessment strategy for small molecule and biologic drug discovery projects from inception to regulatory submission, designing screening cascades and mechanistic experiments. Partner with machine learning researchers to build predictive toxicology models and manage CRO relationships for outsourced wet-lab data generation, while mentoring junior team members.

KNIME · Python

• London
• Hybrid
• Senior

Leads global clinical data transparency and disclosure across registries and regulatory platforms such as CTIS, EMA Policy 0070 and Health Canada PRCI, acting as subject matter expert for assigned therapeutic areas. Manages vendor partnerships, FOI access requests, redaction and lay summary work, plus SOP governance, compliance reporting and audit readiness within Global Regulatory Affairs Excellence.

CTIS · ClinicalTrials.gov · EU Clinical Trial Register +3

• London
• Hybrid
• Lead · manages people

Leads one or more Early Development Asset Teams, owning integrated strategy from candidate nomination through first-in-human trials across preclinical, translational, clinical, regulatory and CMC workstreams. Serves as scientific champion for oncology assets, presenting data and investment recommendations to governance bodies and contributing to in-licensing due diligence.

• London
• Hybrid
• Lead

Leads statistical work for post-marketing clinical trials, observational studies and real world data investigations, serving as Statistics lead on assigned projects. Develops protocols, analysis plans and TFL specifications, collaborating with clinical development, medical affairs, health economics and real world evidence teams. Requires strong SAS and R skills with a drug developer mindset.

SAS · R

• 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

• Cambridge
• Senior
• Temporary

Hands-on upstream process development role delivering mammalian cell culture studies, including CHO-based fed-batch and perfusion processes, media and feed optimization, and bioreactor operation from ambr systems to bench-scale stirred tanks. Works under minimal supervision within a matrix CMC team, applying DoE and statistical analysis, supporting scale-up and tech transfer to GMP and CMO partners, and providing day-to-day technical coordination to technicians and operators.

ambr · ambr250 · Stirred-Tank Bioreactors +6

• Saffron Walden
• Hybrid
• £38,570 – £49,893 pa
• Entry level
• Contract

A postdoctoral research role analysing large-scale human genetic, epigenetic and proteomic datasets, including dried blood spots, birth cohorts and cell-free DNA, to uncover the genetic basis of early-life traits and develop biomarkers for pregnancy and neonatal conditions. The work spans statistical genetics, multi-omics and methods development, with scope to tailor projects to the fellow's interests.

GitHub · Snakemake · Nextflow +1

• Cambridge
• Director · manages people

Lead a biometrics team delivering statistical design, analysis and interpretation for oncology product development, from preclinical studies through regulatory submissions and health technology assessment. Represents statistical strategy at internal governance and external bodies such as health authorities and advisory boards, while mentoring statisticians and partnering with CROs.

SAS · R · Python

• London
• Hybrid
• Director · manages people

Leads the development and execution of international regulatory strategy across European and Rest of World markets, from first-in-human through post-marketing. Represents Global Regulatory Affairs on core development teams, manages project plans and resources, and advises senior management. Also a people manager within the International GRA leadership team, driving process improvement and regulatory policy engagement.

EMA

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

Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare analyses and evaluations for regulatory compliance. Supports Safety Management Teams, conducts proactive safety data reviews, and serves as product point of contact, with hybrid working requiring three days on site.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint