Biotechnology Jobs

• Rockville, United States
• Hybrid · 2–3 days in office
• US$151,500 – US$252,500 pa
• Director

Leads cross-functional project teams within Oncology Translational Medicine, coordinating diagnostics, biomarker and clinical development activities with internal groups and external labs and manufacturers. Manages integrated timelines, budgets, contracts and invoices, tracks milestones and risks, and supports regulatory documentation and technical evaluations of diagnostic technologies.

Microsoft Project · Microsoft Word · Microsoft Excel +7

• Stevenage
• Lead

Leads digital use cases across the CMC portfolio, translating analytical workflows and user needs into business requirements, success criteria and deployed digital solutions. Runs cross-functional teams end to end from concept to go-live, covering business acceptance testing, change management, training and adoption. Sits at the intersection of science, process and technology within GSK's CMC Digitalisation transformation.

Artificial Intelligence · Laboratory Informatics

• Lisburn
• On-site
• Entry level
• Internship

A 12–14 month university placement for penultimate-year students, supporting the Statistical Programming group on clinical trials. Day to day you produce analysis and submission datasets, statistical tables, graphs and data listings using SAS, while learning about the pharmaceutical industry, clinical trial conduct and good clinical practice within a global project team.

SAS · R · MATLAB +1

• United Kingdom
• Remote
• Senior

Clinical Research Associate role within PPD's Functional Service Provider division, dedicated to a client and embedded in multi-national project teams. You perform and coordinate all aspects of clinical monitoring, conducting monitoring activities independently across challenging projects. Requires ICH-GCP, EU and FDA knowledge, with award-winning training provided.

• United Kingdom
• Remote
• Director · manages people

Senior physician role providing metabolic therapeutic and drug-development expertise to a clinical research organisation, supporting major proposals and bid defences, client peer-to-peer engagement, and protocol design. Also trains and mentors internal clinical teams, authors regulatory documents, and liaises with investigators and KOLs. Requires an MD with metabolic subspecialty certification and fluency in English and Mandarin, with travel to China.

• New York, United States
• Remote
• Senior · manages people

Leads clinical development strategy and execution across oncology and rare disease programs, overseeing early and late-stage trials, regulatory interactions, and biomarker-driven study design. Manages teams of clinical scientists and medical directors while embedding AI, machine learning, and real-world data into trial design and evidence generation.

Recursion OS

• New York, United States
• Hybrid
• US$321,800 – US$443,080 pa
• Director · manages people

Sets enterprise strategy for clinical pharmacology, pharmacometrics and model-informed drug development across a clinical portfolio, owning dose strategy from first-in-human through registrational development. Leads quantitative approaches including population PK, PK/PD, PBPK and QSP, represents the company in health authority interactions, and builds a high-performing function within an AI-native TechBio.

Recursion OS

• 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

• London
• Remote
• Senior

Responsible for the successful delivery of clinical studies at assigned investigator sites, acting as the primary point of contact for site management, monitoring, and study execution. Leads site preparation, initiation, routine monitoring, and close-out, conducting onsite and remote visits, source data review and verification, and CRF review while managing risk-based quality and regulatory compliance. Works within a local study team supporting a key sponsor, with travel across the UK and internationally.

CTMS · eTMF

• London
• Hybrid
• Director · manages people

Leads global medical strategy for the Neurosciences portfolio, primarily Dysport Movement Disorders indications, defining evidence generation plans, registries and investigator-sponsored research. Acts as Medical functional lead on the global Asset Team, chairs the Medical & Evidence Generation Team, and represents Ipsen with KOLs, societies and advocacy groups. Also leads, coaches and develops Global Medical Directors across the organisation.

Dysport

• London
• Hybrid
• Mid-level

Drives clinical supply forecasting and IMP budgeting for global trials, translating study protocols and recruitment projections into forecasting tools and monitoring deviations over 3-12 month horizons. Coordinates cross-functional IMP estimation and risk assessment meetings, aligning manufacturing, packaging and distribution to prevent stock-outs, while leading continuous improvement in a matrixed environment.

RTSM · Excel

• Uxbridge
• Director · manages people

Owns the clinical strategy for one or more neuropsychiatry programs, serving as Clinical Trial Physician and clinical point of accountability for the Clinical Development Team. Leads trial design, data interpretation, regulatory submissions and health authority interactions, with matrix leadership across global scientific teams.

• 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

• 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

• Maidenhead
• Mid-level · manages people

Leads the preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Takes a lead role on assigned projects for content, scientific strategy, timing and tracking, and manages direct reports including hiring, goal-setting and development. Involves guiding cross-functional teams, peer review and maintaining knowledge of ICH and regulatory guidelines.