247 jobs for “Analytical Chemical Process Development ”
Drives the development and execution of the analytical network strategy across GSK's global supply chain, defining QC testing network principles and translating them into an operational roadmap. Acts as the single point of contact in GSC Strategy, collaborating with Quality, MSAT and R&D, benchmarking industry practice and reporting KPIs to senior leadership.
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
Basecamp Research
Owns the end-to-end sample-to-sequence pipeline for the Trillion Gene Atlas, spanning DNA extraction, library prep and sequencing dispatch across Phase 1 and Phase 2. Bridges R&D and production by scaling validated protocols, applying Lean/Six Sigma to improve throughput, and leading a small lab team while monitoring data return with bioinformatics partners.
Illumina · Ultima · PacBio +3
Ipsen
Leads global operational delivery of early development oncology programs, managing Clinical Project Managers, Monitoring Leads and CTAs. Owns the clinical development plan, CRO and site selection strategy, budgets and timelines, and serves on Asset Teams. Requires deep first-in-human and Phase I oncology trial expertise.
Microsoft Office
Ipsen
Lead global labelling strategy for assigned products across early and late-stage development, lifecycle management and marketed portfolios, serving as Therapeutic Area Lead. Drive core labelling documents including CCDS, USPI and EU PI, lead health authority negotiations, and shape a future USPI operating model while championing digitalisation and AI-enabled labelling solutions.
FDA · EMA · ICH
Johnson & Johnson Innovative Medicine
A 12-month student placement in the clinical research department, supporting international trials of medical technology products. Duties include administering and coordinating the logistical aspects of clinical studies, tracking essential documents, and collecting and recording study data, with meetings alongside cross-functional partners.
Microsoft Excel · Microsoft Word · Microsoft PowerPoint
IQVIA
Lead the development of country, site and patient enrollment strategies for complex global clinical trials, analysing clinical and operational data to shape feasibility and study delivery. Present recommendations to clients and senior stakeholders, with a particular focus on APAC opportunities including China. Mentors colleagues and acts as subject-matter expert for planning tools.
Genomics
Drive innovation as a strategic consultant on high-impact drug discovery projects with external pharma and biotech partners. Navigate the full development pipeline from target discovery to patient stratification, applying statistical human genetics and large-scale genomic data analysis in R or Python. Partner-facing role translating complex findings into actionable insights.
Genomics
Early-career scientist role in a Life Sciences team, generating therapeutic hypotheses by mining in-house genomic data with statistical methods to identify and triage drug targets. Also develops and optimises polygenic risk score tools for patient stratification, working with omic data using statistical and AI/ML approaches and communicating findings to internal and external stakeholders.
Git · GitHub · WDL +4
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.
Fortrea
Client-facing biostatistics role leading design and analysis of non-interventional and low-interventional studies using real-world data such as claims, EHR and registries. Applies causal inference methods, target trial emulation and synthetic control arms, authors SAPs and manages SAS programming teams, while supporting proposals, budgeting and bid defences.
SAS · CDISC
Fortrea
Owns product strategy, roadmap and innovation for clinical pharmacology clinics and bioanalytical labs, spanning early-phase platforms like ClinSpark, LIMS/LIS, ELN, instrument connectivity and lab automation. Builds business cases and secures funding, governs a regulated portfolio, and leads multidisciplinary product teams and vendors across distributed sites.
ClinSpark · LIMS · LIS +7
IQVIA
Serves as subject matter expert in COA endpoint strategy, instrument development and regulatory strategy, advising pharma and biotech sponsors and representing the company as an external scientific thought leader. Leads qualitative research supporting content validity, oversees internal project teams, mentors consultants and supports business development through proposals and client presentations.
McGregor Boyall
Client-facing consulting role in a global technology consultancy's Data & AI practice, serving pharmaceutical and Life Sciences clients. Combines hands-on Data Science, ML and GenAI delivery with strategy, pre-sales and senior stakeholder engagement, focused on commercial applications such as sales, marketing and customer analytics.
Python · SQL
