Biotechnology Jobs

• Durham Blackwell Street
• Hybrid
• US$204,000 – US$340,000 pa
• Director

Leads the design and delivery of real-world evidence and health outcomes studies for oncology assets, managing protocols, budgets, vendors and reporting from concept to publication. Advises medical, market access and commercial teams on payer and HTA evidence needs, and builds relationships with external experts and data partners.

• USA - Pennsylvania - Upper Providence
• Hybrid
• US$204,000 – US$340,000 pa
• Director

Leads the design and execution of real-world evidence and health outcomes studies across oncology assets, managing timelines, budgets and vendor deliverables. Reviews protocols, analysis plans and publications, and advises medical, market access and commercial teams on payer and HTA evidence needs. Builds relationships with external experts and maintains knowledge of real-world data sources.

• 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.

• 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

• London
• Remote
• Senior

Responsible for the successful delivery of clinical studies at assigned investigator sites, acting as the primary point of contact for site management, monitoring, and study execution. Leads site preparation, initiation, routine monitoring, and close-out, conducting onsite and remote visits, source data review and verification, and CRF review while managing risk-based quality and regulatory compliance. Works within a local study team supporting a key sponsor, with travel across the UK and internationally.

CTMS · eTMF

• London
• Remote
• Senior

Responsible for the successful delivery of clinical studies at assigned investigator sites, acting as the primary point of contact for site management, monitoring, and study execution. Leads site preparation, initiation, routine monitoring, and close-out, conducting onsite and remote visits, source data review and verification, and CRF review. Works within a local study team for a key sponsor, using CTMS, eTMF and risk-based quality management, with travel across the UK and internationally.

CTMS · eTMF

• New York, United States
• Hybrid · 2–3 days in office
• US$124,400 – US$207,400 pa
• Lead · manages people

Leads the strategy, design and lifecycle management of Pfizer's clinical supply chain systems, aligning a 3-5 year product roadmap with Global Clinical Supply objectives. Partners with digital product managers and business SMEs on solution design, process improvement and portfolio prioritisation, reporting metrics to senior leadership. Hybrid role with up to 15% travel.

• Weston-super-Mare
• On-site
• £23 – £24 ph
• Senior
• Temporary

Support the daily operational management of a Clinical Chemistry laboratory, performing routine and specialist testing, result validation, and analyser maintenance. Work with Beckman Coulter DxC700 AU, DxI 800 and DxA Automation Track systems, Remisol middleware and WinPath LIMS, participating in IQC/EQA and ISO 15189 compliance.

Beckman Coulter DxC700 AU · Beckman Coulter DxI 800 · Beckman Coulter DxA Automation Track +2

• Cambridge
• Hybrid · 3 days in office
• Director

Lead digital health strategy engagements with AstraZeneca R&D, top pharma and biotechs, shaping operating models and roadmaps across clinical development. Directs project teams on AI and digital solutions such as ePRO/eCOA, wearables and digital biomarkers, building business cases and tracking value realisation. Combines consulting, protocol design support and scaled implementation in a matrixed environment.

ePRO · eCOA · Wearables +1

• Maidenhead
• Hybrid · 3 days in office
• US$317,000 – US$409,000 pa
• Director · manages people

Leads a cross-functional Clinical Development Team as the lead scientific expert, owning the clinical strategy, plan and medical monitoring for immunoglobulin programs. Accountable for clinical content of regulatory submissions and study documents, and serves as medical monitor across trials in a matrixed environment.

• Opfikon, Switzerland
• Hybrid · 3 days in office
• US$317,000 – US$409,000 pa
• Director · manages people

Leads the cross-functional Clinical Development Team as lead scientific expert, owning the Clinical Development Plan and integrating internal and external contributions into program strategy. Serves as medical monitor, authors key regulatory and study documents, and presents to safety and review committees.

• Cambridge, United States
• Hybrid · 3 days in office
• Director

Lead end-to-end clinical trial material planning, vendor management, packaging, labeling, inventory and global distribution for an AI-first drug discovery company. Act as the clinical supply authority within a lean Pharmaceutical Sciences & CMC team, building scalable systems and vendor networks while partnering closely with Clinical Operations and CROs.

IRT · RTSM

• Uxbridge
• Director · manages people

Owns the clinical strategy for one or more neuropsychiatry programs, serving as Clinical Trial Physician and clinical point of accountability for the Clinical Development Team. Leads trial design, data interpretation, regulatory submissions and health authority interactions, with matrix leadership across global scientific teams.

• Uxbridge
• Director

Serves as primary medical accountability for multiple Phase 1-3 clinical trials in GI oncology, leading medical data review, safety assessment and site interactions within a Study Delivery Team. Partners with Clinical Scientists on protocol design, benefit/risk analysis and health authority interactions, while building relationships with principal investigators and thought leaders.

• United Kingdom
• Remote
• Senior
• Permanent

Provides clinical quality oversight and a single point of Quality contact for client study teams, partnering with Clinical Operations and Pharmacovigilance to identify, assess and mitigate risks to participant safety and reporting compliance. Co-chairs Joint Quality Councils, analyses QA metrics and audit/inspection trends, and drives quality risk management across a portfolio. Fully remote role with up to 25% travel.