Biotechnology Jobs

• USA - Pennsylvania - Upper Providence
• US$139,425 – US$232,375 pa
• Director

Acts as the operational hub for oncology assets, owning the integrated project plan, budget and risk inputs while driving critical-path acceleration and governance decisions. Partners with project leads to navigate uncertainty, facilitate high-performing teams and embed consistent project management practices across the pipeline.

Planisware · MS Project

• Waltham, United States
• US$139,425 – US$232,375 pa
• Director

Acts as the operational 'COO' of a drug or vaccine asset, owning the single integrated project plan and partnering with project leads to steer strategy through complexity. Drives critical-path acceleration, risk management, governance preparation and cross-functional handoffs, with budget and resource forecasting using tools such as Planisware or MS Project.

Planisware · MS Project

• London
• Hybrid
• Director

Lead CMC regulatory strategy for UK-manufactured and UK-licensed mRNA products across development, registration and post-approval lifecycle. Act as primary point of contact with the MHRA, oversee submissions and manufacturing change assessments, and shape global regulatory approaches across cross-functional matrix teams.

MHRA · Generative AI

• 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

• London
• Hybrid
• Lead · manages people

Serves as the clinical trial pharmacy subject matter expert across global oncology programmes, advising on investigational product handling, preparation, storage and accountability, and on hazardous drug and CSTD requirements. Develops pharmacy manuals and training for site pharmacists and study teams, supports audits and CAPAs, and oversees FSP pharmacists and external vendors. Hybrid role spanning London, Paris or Cambridge MA.

Closed System Transfer Devices

• London
• Lead

Ensures clinical trials comply with quality standards, SOPs and health authority regulations, partnering with site management and therapeutic area leads. Builds cluster quality plans, leads CAPA and root cause investigations, and supports audit and inspection readiness across internal and FSP teams. Also handles local regulatory intelligence and supplier quality assessments.

Quality Risk Management System

• London
• Hybrid
• Director
• Permanent

Lead clinical pharmacology and pharmacometrics across a growing drug discovery portfolio, serving as the quantitative lead on cross-functional project teams. Apply MIDD, PBPK, population PK/PD and QSP modelling to translate nonclinical data into human dosing and trial design, spanning small molecules, biologics and novel platforms. Also manages CRO partnerships and authors regulatory submissions.

NONMEM · R · Monolix +3

• Uxbridge
• Hybrid · 3 days in office
• Director · manages people

Leads clinical development strategy for multiple myeloma cell therapy programs, overseeing trial design, conduct, reporting and regulatory submissions. Represents products in governance committees, provides medical monitoring, and manages a team of direct reports while building external thought-leader relationships.

Workday

• Swindon
• Lead · manages people

Leads a team of scientific officers performing GMP QC Chemistry analysis of incoming goods, in-process, intermediate, stability and finished product samples. Acts as first escalation point for technical, compliance and personnel issues, manages batch release, stability studies, documentation and audits, and deputises for the QC Manager. Requires extensive instrumental and traditional analytical experience plus 2+ years of team leadership.

• Oxford
• On-site
• Director · manages people

Lead the DMPK team at Vertex's Oxford site, shaping strategy and operations while sitting on both the Global DMPK and Oxford Site leadership teams. The role directs ADME science across discovery and development programmes, partners with Medicinal Chemistry, Biology, Preclinical Safety and Clinical Pharmacology, and oversees regulatory documentation such as INDs and marketing applications. It combines deep small-molecule DMPK expertise with hiring, mentoring and resource planning.

• London
• Hybrid
• Entry level
• Internship

A 12-month industrial placement within an international Data, Technology and Engineering team, focused on scaling responsible AI adoption, supporting product teams with backlog refinement and delivery, and translating business needs into user stories and requirements. Includes planning an Early Talent Hackathon and business analysis across a regulated biotech environment.

AI Tools

• London
• On-site
• £27,500 – £30,000 pa
• Entry level
• Temporary

Processing blood and other biofluids from volunteer donors in a research services lab, including centrifugation, buffy coat and PBMC separation, reagent preparation and microbiological/viral testing of urine. Work follows Human Tissue Act, ISO 9001 and internal safety standards, with responsibility for maintaining laboratory records. Suited to someone starting out who has some blood or accredited lab experience.

• Manchester

Field-based role selling laboratory reagents and custom/bulk chemicals directly to customers and through top-tier distributors across Northern UK. You build territory plans, forecast, maintain CRM, train sales reps, and support trade shows, working with clients in pharma, food and beverage, and environmental testing. Requires a chemistry background and frequent travel.

CRM

• Norwich
• Hybrid · 3 days in office
• Mid-level
• Contract

You will own the delivery and reporting of two live Innovate UK projects, managing plans, milestones, budgets, risks and financial claims while coordinating consortium partners, funders and scientific teams. Working closely with the CEO, CBO and researchers, you will improve how projects are planned and tracked rather than inheriting a fixed system, and support future grant applications.

Innovate UK · UKRI

• Remote Opportunity - United States; Salt Lake City, Utah
• Remote
• Entry level
• Internship

Join a talent network for future internship opportunities at a clinical-stage TechBio company, with no current openings for Summer 2026. Submit your resume to be considered for upcoming internship rounds, working at the intersection of AI and drug discovery across biology, chemistry, and clinical development.