Biotechnology Jobs

• 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

• 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.

• Reading
• Hybrid
• Mid-level

Supports clinical trials by designing, setting up and maintaining Interactive Response Technology (IRT) solutions, translating supply requirements into system specifications. Contributes to risk assessments, user acceptance testing and validation documentation, and advises study teams on IRT processes. Works with cross-functional global stakeholders on study startup, amendments and continuous improvement.

IRT · RTSM · IVRS +1

• Livingston
• On-site
• Entry level

Assembles clinical trial test kits with specimen collection materials according to protocol, prepares investigator instruction manuals and flowcharts, and packages completed kits with documentation and ancillary supplies for shipment. Monitors inventory levels and alerts supervisors when supplies run low to prevent study delays. Site-based role requiring strong attention to detail and organizational skills.

• 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

• London
• Remote
• Director

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

• Maidenhead
• Mid-level

Conducts and oversees site monitoring visits, managing site initiation, monitoring and closeouts while ensuring patient safety, data integrity and GCP compliance. Supports feasibility assessments, investigator recruitment and vendor coordination, and mentors junior team members. Requires Phase I patient-study experience within a client-dedicated FSP team.

• Maidenhead
• Hybrid
• Mid-level
• Temporary

Monitoring investigator sites across the North of England for a routine post-market surveillance study within a dedicated FSP model. Involves on-site and remote monitoring, building relationships with investigators, and ensuring patient safety, data quality and regulatory compliance, with travel to Oxford at least monthly plus on-site onboarding and training.

• United Kingdom
• Remote
• Lead

Lead medical writer dedicated to a single client, authoring and reviewing clinical study reports, protocols, IBs, INDs and MAAs while advising on document strategy and regulatory requirements. Provides senior review, mentoring and training to junior writers and program managers, and leads process improvement initiatives. Therapeutic experience in neurology, immunology, oncology or vaccines is valued.

• 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.

• London
• Hybrid
• £67,900 – £126,100 pa
• Senior

Co-leads cross-functional Clinical Trial Teams and global studies from planning through close-out, managing timelines, budgets, risks and inspection readiness. Partners across global and local functions on recruitment, data operations and vendor performance, while championing operational excellence and continuous improvement.

• Home Worker - NORTHERN IRELAND
• Remote
• Director · manages people

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.

• London
• Remote
• Mid-level

Manages a portfolio of clinical research studies end to end, leading cross-functional teams and client relationships for Patient Cloud products such as eCOA/ePRO, eConsent and virtual trials. Involves risk assessment, study documentation and milestone tracking, with flexibility needed to work American time zones.

MS Office Suite · Google Workspace

• London
• Hybrid
• Director · manages people

Leads the global and US Medical Affairs Neuro-Oncology team, owning medical strategy, evidence generation and launch planning for pipeline and marketed assets. Serves as a key interface between Medical Affairs and R&D, clinical development and commercial functions, representing regional insights in governance forums. Combines people management with hands-on execution across a complex matrix.

• Gaithersburg, United States
• On-site
• US$218,330 – US$327,494 pa
• Director

Leads competitive intelligence for AstraZeneca's oncology R&D, owning delivery of clinical and commercial analysis that shapes therapy-area strategy and portfolio investment decisions. Works with a specialist team and senior leadership, translating complex data into insights and challenge. Requires oncology, clinical or investment analysis background.