406 jobs for “Pharmaceutical Scientist”
Eurofins
Perform structural elucidation and impurity characterisation of small molecule APIs using advanced mass spectrometry, supporting regulatory submissions and control strategies. Develop Eurofins' MS capabilities, collaborate with cross-functional teams, and work to GLP, cGMP and SHE standards at a client pharmaceutical facility.
Designs disease data information models for priority discovery areas, writing mapping rules to harmonise biomedical data and building quality checks to keep it trustworthy. Works hands-on in code and modelling tools, using AI assistants daily, and partners with research, ontology and data platform teams plus external partners.
NCI Thesaurus · MONDO · EFO +6
GSK · 10000+ people · Public
Leads model-informed drug development for oncology programmes, defining and executing model-based strategies from late pre-candidate selection through life cycle management. Conducts population PK, exposure-response and simulation-based trial design work across small molecules, biologics and antibody drug conjugates, applying AI/ML and quantitative systems pharmacology methods. Presents and defends modelling outcomes to governance boards and regulators, and contributes to protocols, analysis plans and submissions.
NONMEM · R
Join a cross-functional team of scientists, engineers and drug hunters advancing frontier AI research and end-to-end applications across drug discovery, design and translation. Work spans large datasets, multimodal models and virtual cell/virtual patient concepts within one of biopharma's largest AI compute clusters.
AI Compute Clusters
Recursion · 501–1000 people · Series C
Integrate phenomics, transcriptomics, genomics and proteomics data to nominate novel targets and validate immunology and inflammation disease biology, piloting new methods for target discovery and early patient population hypotheses. Partner cross-functionally with biologists, chemists, data scientists and engineers to build data packages that drive program milestones and investment decisions.
Python · R · CRISPR
Evotec
Operate pilot plant reactors and ancillary equipment in a GMP-regulated large-scale chemical production environment, running multiple syntheses, some never previously scaled. Duties include routine maintenance and reconfiguration of reaction vessels, environmental monitoring, accurate batch documentation, and shift handovers. The role follows a rotating 12-hour day and night shift pattern averaging 42 hours per week.
Microsoft Office
Veterinary Medicines Directorate (VMD)
Assesses quality data submitted by companies to support marketing authorisation applications and variations for veterinary medicines, as part of the Quality team within the Pharmaceuticals Section. Also contributes to regulatory science strategy, guideline development, product defect assessment and international training of other regulators.
Microsoft Office 365 · Word · Excel +3
Acts as the primary interface between business stakeholders, biostatisticians, statistical programmers and technical delivery teams, translating clinical and statistical requirements into scalable R-based analytics, automation workflows and enterprise reporting. Leads requirement workshops, manages a small team, and oversees releases with end-to-end traceability, regulatory compliance and audit readiness across the clinical trial lifecycle.
Acts as the primary interface between business stakeholders, biostatisticians, statistical programmers and technical delivery teams, translating clinical and statistical requirements into scalable R-based analytics, automation workflows and enterprise reporting. Leads requirement workshops, manages a small team and oversees releases with end-to-end traceability, regulatory compliance and audit readiness across development, validation and deployment.
AstraZeneca · 10000+ people · Public
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
Parexel
Provides statistical consulting and strategic advice on optimal study designs and analyses across drug, device, and diagnostic clinical development, including preparation for regulatory authority interactions. Serves as a leader in innovative study designs for client accounts and supports new business through proposals, bids, and client presentations, representing clients at key regulatory meetings.
FDA · EMEA · MHRA +2
Thermo Fisher Scientific
Supports clinical trial delivery by coordinating site activation, maintaining (e)TMF files, tracking regulatory documents and study metrics, and handling finance tasks such as raising POs, vendor setup, invoicing and budget tracking in systems like CERPS, Ariba, Fiori and Veeva Payments. Works within a global FSP team, liaising with investigators and site staff, conducting feasibility assessments and training new personnel.
MS Office · Word · Excel +7
Thermo Fisher Scientific
Lead a medical information operations team, overseeing the development and dissemination of accurate medical and drug information while ensuring regulatory compliance. Responsibilities include supervising staff, quality review of medical/clinical work, client reporting, training, and acting as liaison between clients and program staff. Requires proficiency in English and French.
Talentmark
Process, analyse and interpret omics data from clinical portfolio studies to uncover biological mechanisms, treatment effects and safety signals. Develop analysis pipelines using state-of-the-art tools, document reproducible code for patient-level data, and write reports and scientific publications. Requires strong bulk and single-cell RNAseq expertise, R, HPC/Unix and Docker skills.
Docker · DNAnexus
Isomorphic Labs · 201–500 people · Series A
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
