Biotechnology Jobs

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$222,750 – US$371,250 pa
• Director · manages people

Provides clinical and scientific leadership across cardiovascular clinical development programs, designing CDPs, study protocols and regulatory documents while overseeing medical monitoring and participant safety. Leads a cross-functional Clinical Matrix Team, partners with biology, translational sciences, regulatory and commercial groups, and serves as clinical point of contact for regulators, investigators and key experts. Hybrid role with at least two on-site days per week.

• Upper Providence
• Hybrid · 2 days in office
• US$202,500 – US$371,250 pa
• Director · manages people

Leads clinical development strategy for hepatology assets within the Respiratory, Immunology & Inflammation Research Unit, from target identification through proof-of-concept studies. Accountable for clinical matrix team leadership, protocol design, medical monitoring and safety governance, and regulatory interactions across all development phases.

• Reading
• Mid-level · manages people

Leads end-to-end delivery of regional and global clinical trials embedded within a sponsor's team, managing timelines, budgets, risk and cross-functional groups. Also supports bid defence presentations, vendor management and financial forecasting, mentoring less experienced project team members.

IQVIA

• Reading
• Mid-level

Shapes and drives end-to-end clinical trial supply strategy, translating study protocols into kit designs, demand forecasts and packaging plans. Oversees vendors, IRT systems, distribution and temperature-excursion management while leading client and vendor meetings. Combines analytical planning with operational leadership across GxP-regulated clinical supply work.

Interactive Response Technology · Microsoft Word · Microsoft Excel +1

• Harrow
• Remote
• Lead · manages people

Acts as functional lead on the core project team, driving site identification and country selection for clinical trials from award onwards. Designs protocol-specific site questionnaires, leads local teams through surveys, models enrolment scenarios, and presents data-driven strategies to sponsors. Also serves as SME for feasibility systems and may lead stand-alone feasibility studies.

• Sheffield
• Remote
• Lead

Configures, tests and maintains electronic Clinical Outcome Assessment studies in platforms such as Medidata Designer eCOA, translating protocols and licensed instrument requirements into questionnaires, schedules and branching logic. Acts as technical contact for sponsors and vendors, coordinates eCOA-to-EDC integration and deployment, and mentors less-experienced study designers across multiple global trials.

Medidata Designer eCOA · Medidata Rave

• United Kingdom
• Remote
• Entry level

Supports clinical trial site management remotely, liaising with CRAs and study teams on site preparedness, document collection, vendor trackers and remote monitoring tasks. Handles essential documents, site payments, reconciliations and centralized monitoring reviews in line with SOPs and ICH GCP. Suits an early-career life sciences graduate seeking a UK-based remote clinical research role.

EMR · EHR · CTMS +2

• Maidenhead
• Senior

Lead and manage clinical trial sites across a diverse portfolio spanning oncology, neuroscience, cell & gene and CAR-T therapies. The role emphasises patient safety, data integrity and building trusted relationships with investigators, with autonomy and support for complex, innovative study designs.

• Maidenhead
• Mid-level

Monitors clinical trial sites across a diverse portfolio spanning oncology, neuroscience, general medicine, cell & gene and CAR-T therapy. Leads site management, builds relationships with investigators and study teams, and safeguards patient safety and data integrity on complex, first-in-class studies. Distinct for its breadth across therapeutic areas and advanced therapy exposure rather than a narrow single-indication focus.

• Opfikon, Switzerland
• Hybrid · 3 days in office
• US$212,000 – US$251,000 pa
• Director

Leads the full statistical contribution to a clinical development programme, defining statistical strategy for trial design, analysis and regulatory submissions, and representing Biostatistics in interactions with the FDA, EMA and PMDA. Also manages outsourcing to CROs and internal statistical programmers, and supports departmental improvement initiatives.

SAS · R

• United Kingdom
• Remote
• Lead · manages people

Leads global regulatory strategy for Phase 1-4 clinical trials, preparing and assembling CTA submissions and acting as the client-facing liaison with sponsors and regulatory agencies. Represents the regulatory department in bid defense and launch meetings, managing project teams and reviewing clinical and scientific documentation.

Microsoft Word · Microsoft Excel · PowerPoint

• Dublin, Ireland
• Hybrid
• €63,600 – €118,000 pa
• Lead · manages people

Lead and develop a team of Central Monitors while shaping risk-based monitoring strategies across a global clinical development portfolio. Oversee trial-data surveillance, signal detection and insight generation, translating complex risk signals into actionable insights and designing study-specific Key Risk Indicators and Quality Tolerance Limits.

Artificial Intelligence

• Hyderabad, India
• On-site
• 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 the clinical trial lifecycle.

• Newcastle upon Tyne
• £21,805 pa
• Entry level
• Contract

Investigates the molecular mechanisms of liver dysfunction in childhood POLG-related mitochondrial disease, focusing on Alpers-Huttenlocher syndrome. Uses quantitative untargeted proteomics and immunohistochemistry on donated post-mortem liver tissue, and generates hepatic organoids from patient-derived iPSCs for disease modelling and therapeutic screening. Based in the Newcastle Mitochondrial Research Group with a placement at the University of St Andrews.

iPSCs

• London
• Remote
• Mid-level
• Permanent

Field-based medical affairs role acting as a scientific partner to healthcare professionals and thought leaders across the East Midlands, Yorkshire and East of England. Involves non-promotional scientific exchange, medical education, advisory boards, and supporting investigator-sponsored and real-world evidence studies within a neuroscience portfolio, working closely with UK, Ireland and global teams.

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