Biotechnology Jobs

• Zug, Switzerland
• On-site
• US$222,750 – US$371,250 pa
• Director

Serves as the physician within oncology clinical programme teams for lung and head/neck cancers, leading medical monitoring, safety oversight and clinical data interpretation. Partners with the Senior Scientist and cross-functional teams on protocol development, regulatory interactions and investigator engagement, with on-site presence 2-3 days per week.

AI-enabled insights

• London
• On-site
• US$222,750 – US$371,250 pa
• Director

Serves as the physician within oncology clinical programme teams for lung and head/neck cancers, leading medical monitoring, safety oversight and clinical data interpretation across Phase I–III studies. Partners with Senior Scientists and cross-functional matrix teams on protocol development, regulatory interactions and investigator engagement, with on-site presence 2–3 days per week.

AI

• Livingston
• Senior

Conducts site qualification, initiation, monitoring and close-out visits for a dedicated sponsor program, ensuring GCP compliance, patient safety and data integrity. Builds investigator relationships, drives recruitment and retention, and mentors junior team members, with up to 40-60% regional travel.

Investigator Site Files (ISF) · Trial Master Files (TMF)

• Manchester
• Senior

Conducts site qualification, initiation, monitoring and close-out visits for a dedicated sponsor program, ensuring GCP compliance, patient safety and data integrity. Builds investigator relationships, resolves queries, mentors junior staff and supports recruitment and start-up activities, with up to 40-60% regional travel.

Investigator Site Files (ISF) · Trial Master Files (TMF)

• Kingsfold
• On-site
• £16 ph
• Entry level
• Temporary

Picking and packing client orders, receiving courier deliveries into inventory software, and following production orders for packaging in a GMP-regulated pharmaceutical environment. Involves cycle counts, waste disposal, SOP compliance and continuous improvement, working in ambient, refrigerated and frozen conditions down to -20°C.

Inventory Software

• London
• Hybrid
• £47,540 – £88,289 pa
• Mid-level

Manage regulatory activities for clinical trial applications across an assigned portfolio, working with study teams, country leads and cross-functional partners. Anticipate regulatory risks, coordinate responses to Health Authority queries and maintain product information in compliance systems, while contributing to automation and simplification initiatives.

• Home Worker
• Remote
• £47,540 – £88,289 pa
• Mid-level

Manages regulatory activities for clinical trial applications across an assigned portfolio, leading high-quality submissions and coordinating responses to Health Authority queries. Works closely with study teams, country leads and cross-functional partners to identify regulatory risks early and secure timely approvals, while contributing to simplification and automation initiatives across Regulatory Affairs.

• 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

• Leeds
• Hybrid
• Senior
• Permanent

Leads data management activities across early phase trials, including healthy volunteer and patient populations, multi-site studies and reduced timelines. Accountable for all DM deliverables, resource allocation, client relationships and scope changes, while mentoring the internal study team and adopting new DM technologies.

• Maidenhead
• Hybrid
• Senior

Leads clinical data management for one or more oncology studies within a sponsor-dedicated (FSP) model, acting as the primary client contact from study set-up through close-out. Combines strategic oversight of vendors, budgets and CDM deliverables with hands-on work such as eCRF design and data cleaning, collaborating with data coordinators and statistical programmers.

eCRF

• 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.

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

Leads competitive intelligence for AstraZeneca's oncology pipeline, delivering clinical and commercial analysis that shapes therapy-area strategy and investment decisions. Partners with senior leadership and cross-functional teams, providing respectful challenge and insight into the evolving oncology landscape. Requires oncology, clinical research or investment analysis background with strong communication and influence skills.

• Harrow
• Remote
• Mid-level

Manage worldwide post-approval regulatory activities for biological and plasma products, focusing on CMC variations, renewals, market expansions and annual reports. Assess change controls, review quality control and production study reports, and coordinate submission content with manufacturing, supply chain and QA teams. Client-dedicated role working in Regulatory Information Management systems such as Veeva Vault.

Veeva Vault · Word · PowerPoint +1

• IM92AP
• On-site
• £29,000 – £32,000 pa
• Mid-level
• Permanent

The QC Analyst role involves performing quality control testing of raw materials, intermediates, and finished products in a regulated manufacturing environment. Responsibilities include analytical testing, environmental monitoring, and maintaining compliance with GMP standards. The role offers exposure to a variety of analytical techniques and technologies, supporting continuous improvement initiatives.

• 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