Biotechnology Jobs

• Warsaw, Poland
• Hybrid · 2 days in office
• PLN 472,500 – PLN 787,500 pa
• Director

Serves as the physician within an oncology clinical program team, leading medical monitoring and safety oversight for genitourinary cancer studies. Interprets clinical and safety data, contributes to protocol development and regulatory interactions, and acts as a core member of the Clinical Matrix Team. Hybrid working with at least two days per week on-site.

AI

• Mississauga, Canada
• Hybrid · 2 days in office
• US$189,750 – US$316,250 pa
• Director

Serves as the physician within oncology clinical program teams, leading medical monitoring, safety oversight and clinical data interpretation for genitourinary studies. Partners with the Senior Scientist and cross-functional Clinical Matrix Team on protocol development, investigator and KEE engagement, and regulatory interactions. May guide other physicians on complex multi-study programmes.

AI

• 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.

• Harrow
• Remote
• Senior

Monitors clinical trial sites across the UK as the sole point of contact, conducting qualification, initiation, monitoring and termination visits and producing visit reports. Manages site quality, regulatory documentation and drug accountability while developing recruitment strategies to meet enrolment timelines. Fully decentralised role with less travel and a lower protocol load than industry peers.

Clinical Trial Management System · Electronic Document Management System · Excel +1

• Manchester
• Mid-level

Conducts site qualification, initiation, monitoring and close-out visits for clinical trials, ensuring GCP compliance, patient safety and data integrity. Builds relationships with investigators, resolves data queries, mentors junior staff and travels up to 40-60% within the region. Embedded in a sponsor-dedicated functional service partnership model.

Investigator Site Files · Trial Master Files

• Bath
• Mid-level

Conducts site qualification, initiation, monitoring and close-out visits for a CRO embedded within pharmaceutical sponsor teams, ensuring GCP compliance, patient safety and data integrity. Manages site relationships, recruitment strategies, TMF/ISF documentation and risk escalation, with mentoring of junior staff and up to 40-60% regional travel.

Investigator Site Files · Trial Master Files

• 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.

• London
• Hybrid
• £67,900 – £126,100 pa
• Senior

Co-leads cross-functional Clinical Trial Teams and global studies from planning through close-out, managing timelines, budgets, risks and inspection readiness. Partners across global and local functions on recruitment, data operations and vendor performance, while championing operational excellence and continuous improvement.

• London
• Remote
• Mid-level

Manages a portfolio of clinical research studies end to end, leading cross-functional teams and client relationships for Patient Cloud products such as eCOA/ePRO, eConsent and virtual trials. Involves risk assessment, study documentation and milestone tracking, with flexibility needed to work American time zones.

MS Office Suite · Google Workspace

• Remote Opportunity - United States
• Remote
• Lead

Join a cross-functional team of scientists, engineers and drug hunters advancing frontier AI research and end-to-end applications across drug discovery, design and translation. Work spans large datasets, multimodal models and a unifying biomedical world model bridging virtual patient and virtual cell, with rapid iteration in an AI-native TechBio environment.

• Remote Opportunity - United States
• Remote
• Senior

Join a cross-functional team of scientists, engineers and drug hunters advancing frontier AI research and end-to-end applications across drug discovery, design and translation. Work spans large datasets, multimodal models and virtual cell/virtual patient concepts within one of biopharma's largest AI compute clusters.

AI Compute Clusters

• United Kingdom
• Remote
• Senior

Acts as independent Principal Investigator overseeing qualitative in-trial research studies, from design through delivery, for pharmaceutical clients. Applies methods like interviews and surveys to capture patient experience data, manages project budgets and timelines, and contributes to proposals and client development. Requires CAQDAS expertise and strong scientific writing.

Atlas.ti · NVivo · MAXQDA +1

• Cambridge
• Director · manages people

Lead a biometrics team delivering statistical design, analysis and interpretation for oncology product development, from preclinical studies through regulatory submissions and health technology assessment. Represents statistical strategy at internal governance and external bodies such as health authorities and advisory boards, while mentoring statisticians and partnering with CROs.

SAS · R · Python

• Haywards Heath
• Hybrid · 3 days in office
• Director · manages people

Leads a global team of development and regulatory project managers overseeing complex R&D programs across a therapeutic area, including new product development and life cycle management. Drives portfolio planning, risk assessment, and cross-functional alignment as part of the Portfolio & Operations Excellence leadership team, with hands-on coaching and process improvement.

Microsoft Project · Planview · Smartsheet +1

• Cambridge, United States
• Hybrid · 3 days in office
• Senior · manages people

Experienced medicinal chemists lead portfolio drug discovery projects from initiation to clinical candidate selection, working as Project Lead or Medicinal Chemistry Lead. They partner closely with ML scientists to refine the AI drug design platform, manage CRO resources, and may line-manage teams of 2-4 chemists.

AlphaFold