Biotechnology Jobs

500 jobs for “Clinical Supply Irt Specialist”

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GSK logo

GSK · 10000+ people · Public

Medical Director-Oncology Clinical Development - GI

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  • Zug, Switzerland
  • Hybrid · 2–3 days in office
  • US$222,750 – US$371,250 pa
  • Director

Serves as the physician within a clinical programme team, leading medical monitoring, safety oversight and data interpretation for GI oncology studies. Partners with a Senior Scientist and cross-functional matrix teams on protocol development, regulatory interactions and investigator engagement. Requires an on-site presence 2-3 days a week across UK, Swiss or US sites.

AI-enabled Insights

3 weeks ago
GSK logo

GSK · 10000+ people · Public

Medical Director Clinical Development- Aging

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  • Waltham, United States
  • Hybrid · 2 days in office
  • US$189,750 – US$316,250 pa
  • Director · manages people

Provides clinical and scientific leadership across early-phase clinical development programs in GSK's Respiratory, Immunology & Inflammation Research Unit, focusing on aging. Leads the Clinical Matrix Team, designs clinical development plans and study protocols, oversees medical monitoring and safety, and represents programs in regulatory interactions. Works cross-functionally with biology, translational sciences, commercial, and regulatory partners.

Last month

IQVIA

Principal Scientist - Cardiac Electrophysiology & Translational Ion Channels

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  • Cambridge
  • Lead · manages people

Lead scientific strategy for cardiac electrophysiology and translational ion channel research, acting as scientific lead across multiple integrated drug discovery programmes. Guide experimental design using automated patch clamp (Qube/Sophion), MEA systems and hIPSC-derived cardiomyocytes, while serving as primary client contact and mentoring scientists.

Qube · MEA Systems · Sophion

Last month

IQVIA

Senior Technical Specialist - DMPK

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  • Cambridge
  • Hybrid
  • Senior

Hands-on bioanalytical role developing, optimising and running LC-MS/MS assays for small and large molecule DMPK studies in an early discovery setting, analysing matrices such as plasma, blood, brain, bile, faeces and urine. Combines complex mass spectrometry troubleshooting and method development with leading scientific projects, mentoring colleagues and driving novel assay innovation in a matrix team.

UPLC-MS · LC-MS/MS · Mass Spectrometry

2 months ago
Isomorphic Labs logo

Isomorphic Labs · 201–500 people · Series A

Research Leader (Toxicology), London

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  • London
  • Hybrid · 3 days in office
  • Lead

Owns safety assessment strategy for drug discovery projects from inception to regulatory submission, working with small molecule and biologics platforms. Designs screening cascades, authors IND packages, and manages CRO relationships for outsourced wet-lab work. Also guides development of an AI predictive toxicology platform with ML researchers.

AI/ML · AlphaFold

3 weeks ago
Novartis logo

Novartis

Senior Scientific Engagement & Program Manager

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  • London
  • Hybrid
  • Senior

Plans and executes medical and scientific engagement activities such as advisory boards, congress symposia, external expert engagements and medical education programmes across oncology, cardiovascular, renal, neuroscience and immunology. Works within the International Medical Affairs Center of Excellence, translating engagement strategy into operational plans, managing vendors, logistics and budgets, and reinforcing compliant, audit-ready ways of working.

CRM Software

3 weeks ago

Evotec

VP Head of Therapeutics Design

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  • Abingdon
  • On-site
  • Director · manages people
  • Permanent

Owns Evotec's in silico therapeutics design capability, uniting computational chemistry, generative and modality design (small molecules, peptides, protein engineering, degraders, molecular glues) and predictive ADMET/safety under one mandate. A newly created unit within the In Silico & AI group with an explicit build mandate: set technical vision, grow a multi-site team, and industrialise repeatable, benchmarked methods across partner programmes.

RDKit · Python · AlphaFold

3 weeks ago

Gilead Sciences

Sr Director, Medical Writing

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  • Cambridge
  • Director · manages people

Leads a team of medical writers and oversees strategic planning and drafting of complex regulatory submissions at the therapeutic area or portfolio level. Acts as subject matter expert, driving document strategy with cross-functional teams across Regulatory Affairs, Clinical Research and Clinical Data Science, plus process improvement and training initiatives.

Workday

Last month

Mytos

Principal Scientist (PD/MSAT)

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  • London
  • Lead · manages people

Provides technical leadership in setting up and operating a CDMO site, leading process development and analytical method development projects for cell therapy manufacture. Plans technology transfers, ensures regulatory compliance, drives continuous improvement, and mentors colleagues while engaging directly with clients.

MHRA · EMA · FDA

5 months ago

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