Biotechnology Jobs

• Baar Onyx
• Hybrid
• US$204,000 – US$340,000 pa
• Director

Leads the design and execution of real-world evidence and health outcomes studies for oncology assets, managing timelines, budgets and quality of protocols, analyses and publications. Advises internal medical, market access and commercial teams and external experts on evidence strategy for HTA submissions, reimbursement and value-based pricing. Requires deep knowledge of RWD sources and payer evidence needs.

• London
• Director · manages people

Owns the strategy, organization and delivery of data and data science capabilities across R&D, leading a portfolio of R&D Data Categories through Senior Technical Data Product Owners. Sets governance and delivery standards while spending at least half the time hands-on writing code, building models and developing agentic AI systems for trusted data-science work.

OpenAI · CDISC SDTM · CDISC ADaM +2

• Reading
• Mid-level

Embedded with a global pharmaceutical sponsor, you act as the clinical supply representative in cross-functional study teams, owning supply strategy, vendor oversight and risk mitigation. Work spans protocol interpretation, label text, demand forecasting, packaging campaigns, IRT setup and temperature excursion management, with a strategic rather than operational focus.

IRT · RTSM · ERP +4

• Manchester
• Mid-level

Conducts site qualification, initiation, monitoring and close-out visits for clinical trials, ensuring GCP compliance, patient safety and data integrity. Builds relationships with investigators, resolves data queries, mentors junior staff and travels up to 40-60% within the region. Embedded in a sponsor-dedicated functional service partnership model.

Investigator Site Files · Trial Master Files

• Harrow
• Hybrid
• Mid-level

Drives strategic impact by developing operational and technical solutions for Early Phase clinical trials, collaborating with Enterprise Accounts, Growth Accounts, Commercial Operations and Strategic Business Units. Contributes to business development from opportunity identification through solution design, bid strategy and client engagement, crafting differentiated value propositions and proposal content. Requires 3-5 years of Early Phase Clinical Trials experience and up to 30% travel.

Clinical Trial Management Systems · Proposal Development Platforms · Enterprise Software Solutions

• Uxbridge
• Director

Serves as primary medical accountability for Phase 1–3 clinical trials in neuroscience, leading medical monitoring, safety assessment and benefit/risk analysis within a matrixed study delivery team. Partners with clinical scientists on protocol design, site interactions and health authority submissions, and builds relationships with principal investigators and thought leaders.

• Uxbridge
• Director · manages people

Leads clinical strategy and execution for one or more GI oncology indications of a given asset, owning the Target Product Profile and disease area strategy. Manages a team of physicians and scientists designing, running, analysing and interpreting all clinical studies, and acts as internal and external clinical authority for regulatory interactions and business development. Requires deep therapeutic expertise and 8+ years of drug development experience, with international and domestic travel.

• High Wycombe
• Entry level
• Internship

A 12-month industry placement within the Integrated Data Analytics and Reporting function, focused on Clinical and Statistical Programming. The student applies SAS, R, Python, RPA and Power Automate to analyse trial data, build AI-driven tools and automate clinical reporting, while collaborating with programming experts across disease areas.

SAS · R · Python +4

• Oxford
• Hybrid · 3–4 days in office
• Director

As an individual contributor in the Clinical Pharmacology group, you will develop quantitative strategies for dose selection, PK/PD characterization and regimen optimization across oncology, immunology and rare disease programs. You will partner with Pharmacometrics and QSP colleagues, represent CQP on program teams, and contribute to regulatory documentation and interactions.

R · Phoenix WinNonlin · NONMEM +2

• Oxford
• On-site
• Entry level
• Temporary

Support assay development, qualification, validation and clinical sample testing within Moderna's Immunoassay group, generating bioanalytical data that informs clinical trials. Work is primarily lab-based (≥85% of time) under a study lead, with responsibility for data integrity, reagent preparation, equipment upkeep and compliance with GCP/ISO standards.

GraphPad Prism · LIMS · Word +2

• London
• Hybrid
• Director
• Permanent

Lead clinical pharmacology and pharmacometrics across a growing drug discovery portfolio, serving as the quantitative lead on cross-functional project teams. Apply MIDD, PBPK, population PK/PD and QSP modelling to translate nonclinical data into human dosing and trial design, spanning small molecules, biologics and novel platforms. Also manages CRO partnerships and authors regulatory submissions.

NONMEM · R · Monolix +3

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

Leads clinical development strategy for multiple myeloma cell therapy programs, overseeing trial design, conduct, reporting and regulatory submissions. Represents products in governance committees, provides medical monitoring, and manages a team of direct reports while building external thought-leader relationships.

Workday

• Leeds
• Director · manages people

Executive leadership role owning QA and regulatory compliance for the Clinical Pharmacology Services unit, covering CPU operations, GMP pharmacy activities and Phase IB/IIA early-phase trials. Sets risk-based quality strategy, inspection readiness and audit programs, leads global matrixed QA teams and represents the company externally on GCP/GMP matters.

• Cambridge
• Hybrid · 3 days in office
• Director

Provides medical and scientific leadership across late-stage respiratory and immunology clinical programs, from Phase IIb to Phase IV. Involves designing, executing and interpreting pivotal trials, medical monitoring, regulatory document input and building relationships with external scientific experts in an international team.

• Leeds
• Director · manages people

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