Biotechnology Jobs

• Zug, Switzerland
• On-site
• US$284,250 – US$473,750 pa
• Director

Leads clinical development for GU oncology assets, designing and executing Phase 1-3 interventional trials and serving as a core member of the Clinical Matrix Team. Provides real-time medical monitoring, safety review with pharmacovigilance, and authors clinical study reports and regulatory responses. Builds external expert relationships and represents the company at advisory boards and medical meetings.

• USA - Pennsylvania - Upper Providence
• On-site
• US$284,250 – US$473,750 pa
• Director

Leads clinical development of GU oncology assets, designing and executing Phase 1-3 interventional trials and serving as a core member of the Clinical Matrix Team. Provides real-time medical monitoring, safety data review with pharmacovigilance, and authors clinical study reports and regulatory responses. Builds key external expert relationships and contributes to business development diligence.

• 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)

• United Kingdom
• Remote
• Senior · manages people

Accountable for delivering clean clinical data on time and within contract for low-to-moderate complexity haematology/oncology trials, managing operational and quality aspects in line with ICH GCP. Develops monitoring plans, CRF documents and Trial Master File content, tracks timelines and metrics, and may handle start-up, ethics submissions and project financials. Works within a team of CTMs, with travel to sites and a focus on radiopharmaceuticals, cell & gene therapy and CAR-T studies.

Outlook · Excel · Word

• Maidenhead
• Lead · manages people

Provides medical and scientific expertise on clinical safety across the full product lifecycle, with emphasis on evaluating safety data during clinical development and post-approval. Chairs the Safety Management Team, oversees signal detection, aggregate reports (DSURs, PSURs, RMPs) and regulatory responses, and sets safety strategy for global cross-functional development and post-marketing teams.

DSUR · PSUR · RMP +2

• Opfikon, Switzerland
• Lead · manages people

Provides medical and scientific expertise on clinical safety across a product's lifecycle, with emphasis on signal detection, risk management and regulatory submissions. Chairs the Safety Management Team, oversees aggregate reports such as DSURs, PSURs and RMPs, and acts as the safety representative in cross-functional development and post-marketing teams.

DSUR · PSUR · RMP +3

• Oxford
• Hybrid · 3–4 days in office
• Lead
• Permanent

Provides scientific and hands-on leadership for immunogenicity and ligand binding assay bioanalysis supporting mRNA-LNP therapeutic programs, spanning assay development, validation, clinical sample testing and regulatory submissions. Ensures GcLP compliance and partners with cross-functional teams, with opportunities to work alongside data and AI-enabled analytical approaches.

ECL · Gyrolabs · Reporter Gene Assays +3

• London
• Mid-level
• Permanent

Deliver and maintain UK competitive licences, lead regulatory strategy for new initiatives, and ensure compliance across defined products and projects. Provide local regulatory expertise for clinical trial approvals, lifecycle submissions and MHRA interactions, contributing to cross-functional teams and study feasibility work.

Veeva · AI

• Harrow
• Remote
• Senior

Senior regulatory affairs consultant role focused on CMC writing and variations strategy for vaccines and biological products. You will draft CMC sections and scientific rationales for submissions, coordinate activities across multiple projects, liaise with global affiliates and manufacturing sites, and manage client relationships on a dedicated project without people-management duties. Work is home or office based across various European locations.

FDA · EMA · MHRA

• United Kingdom - Walton Oaks
• Senior

Conduct strategic regulatory activities for assigned products and markets, managing Marketing Authorisation applications, variations, renewals and NRA queries. Work with cross-functional teams and above-country hubs to maintain compliance, support clinical trial applications and share regulatory intelligence.

• London
• Remote
• Director

Medically responsible at trial level across preparation, conduct and reporting phases, providing medical expertise and oversight from Trial Design Outline to Clinical Trial Report. Dedicated to a single sponsor in the EMEA region, the role involves authoring high-quality clinical trial protocols, co-authoring Clinical Quality Monitoring plans, integrating medically relevant data into risk-based quality management, and performing ongoing reviews of medical data.

• London

Act as a self-employed field sales agent promoting point-of-care diagnostic solutions to healthcare providers including care homes, pharmacies, and GP practices. Leverage existing relationships to sell diagnostic devices and reagent cartridges, supported by full training and biomedical expertise. Generate income through upfront and recurring commissions from consumable sales.

• London
• Hybrid
• £67,900 – £126,100 pa
• Lead · manages people

Lead and develop a global regulatory team delivering clinical trial submissions and approvals, combining people leadership with regulatory expertise. Drive process improvement, simplification and automation while building stakeholder partnerships across Regulatory Affairs. Hybrid role with remote option for UK candidates over 50 miles from the London office.

• 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.