Biotechnology Jobs

• USA - Pennsylvania - Upper Providence
• 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 a Senior Scientist and cross-functional matrix teams on protocol development, regulatory interactions and investigator engagement, with on-site presence 2–3 days per week.

AI-enabled Insights

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$189,750 – US$316,250 pa
• Director

Serves as the physician within a clinical program team, leading medical monitoring and safety oversight for genitourinary oncology studies. Interprets clinical and safety data, contributes to protocol development and regulatory interactions, and acts as a core member of the Clinical Matrix Team. May guide other physicians on complex multi-study programs.

AI

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

Senior physician leader providing medical oversight, safety evaluation and clinical data interpretation across sarcoma oncology studies, from protocol design through regulatory interaction. Serves as a senior member of the Clinical Matrix Team, mentoring Medical Directors and engaging external experts, with a minimum two-day on-site office presence.

Real World Evidence

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

Senior physician leader providing medical oversight, safety monitoring and clinical data interpretation across sarcoma oncology studies, from protocol design through regulatory interactions. Serves as a senior member of the Clinical Matrix Team, mentoring Medical Directors and engaging external experts, advisory boards and health authorities.

Real World Evidence (RWE)

• London
• Hybrid
• Lead

Lead programming activities for one or more clinical studies, developing, maintaining and validating complex analysis packages to CDISC and Good Programming Practice standards. Act as technical mentor to junior programmers and lead programming support for regulatory interactions with the EMA and FDA. Works in an agile, squad-based team bridging scientific requirements with technical solutions, with R proficiency preferred.

R

• Stevenage
• Hybrid
• Lead

Leads statistical programming for complex and pivotal clinical studies, developing, maintaining and validating analysis packages while ensuring compliance with Good Programming Practices and CDISC standards. Acts as a technical mentor to junior programmers and leads programming support for regulatory interactions with bodies such as the EMA and FDA, working in an agile, squad-based team alongside clinical, statistical and operational stakeholders.

R

• USA - Pennsylvania - Upper Providence
• Hybrid
• Lead

Lead programming activities for complex and pivotal clinical studies, developing, maintaining and validating analysis packages while ensuring compliance with Good Programming Practices and CDISC standards. Mentor junior programmers, support regulatory interactions with EMA and FDA, and bridge scientific requirements with technical solutions in an agile, squad-based global team.

R

• Stevenage
• Hybrid · 2–3 days in office
• Senior

Sits within GSK's Chemical Manufacturing & Control function, identifying and sizing AI opportunities across process development science for oligonucleotides, ADCs and monoclonal antibodies. Partners with forward deployed engineering pods to turn ambiguous business problems into scoped, buildable products, and shapes self-driving lab and in silico modelling initiatives.

Self-Driving Labs · Agentic Workflows · Physical AI

• London
• Hybrid · 2–3 days in office
• Senior

Sits within GSK's CMC function, identifying and sizing AI opportunities across process development science for oligonucleotides, ADCs and monoclonal antibodies. Partners with forward deployed engineering pods to turn ambiguous business problems into scoped, buildable products, and shapes self-driving lab and in silico modelling initiatives.

AI Platforms · ML Platforms

• London
• Hybrid · 2–3 days in office
• Senior

Embedded with chemical manufacturing teams, you take AI use cases from problem framing to working prototypes at days-to-weeks cadence, building in-silico process models, digital twins and optimization solutions. Work is AI-augmented, with coding agents handling routine development while you supply judgement, validation and model identification. Proven solutions are packaged for handoff to a solutions engineer for scale-up.

Claude Code · GitHub Copilot · Databricks AI Assistant +6

• Stevenage
• Hybrid · 2–3 days in office
• Senior

Embedded with chemical manufacturing teams, you build in-silico process models, digital twins and optimization solutions, taking proofs of concept to deployed MVPs at a days-to-weeks cadence. Work is AI-augmented, with coding agents handling routine development while you focus on model identification, scenario planning and handing proven solutions to solutions engineers.

Claude Code · GitHub Copilot · Databricks AI Assistant +4

• London
• Hybrid
• PLN 318,000 – PLN 530,000 pa
• Director

Supports patient safety worldwide by leading signal detection, safety evaluation and risk management for products in clinical development and post-marketing. Prepares global regulatory reports and risk management plans, supports safety governance meetings, and contributes to risk-reduction strategies across cross-functional matrix teams.

Safety Databases · Data Visualisation Tools

• Warsaw, Poland
• Hybrid
• PLN 318,000 – PLN 530,000 pa
• Director

Leads signal detection and evaluation for assigned products, prepares global regulatory reports and risk management plans, and supports safety governance meetings across clinical and post-marketing settings. Works in cross-functional matrix teams, contributes to risk-reduction strategies, and mentors colleagues while driving process improvements in pharmacovigilance.

Safety Databases · Data Visualisation Tools

• London
• Director

Provides advanced scientific expertise in safety evaluation and risk management for key oncology assets in clinical development, leading signal detection, benefit-risk assessment and regulatory safety submissions. Represents the Safety Evaluation & Risk Management function on cross-functional clinical matrix and project teams, escalating emerging safety issues to senior governance. Mentors junior staff and partners with Safety Physicians to shape long-term safety strategy.

• Poznan Grunwaldzka
• PLN 525,750 – PLN 876,250 pa
• Director

Provides advanced scientific expertise in safety evaluation and risk management for key oncology assets in clinical development, leading signal detection, benefit-risk assessment and regulatory safety submissions. Represents SERM on cross-functional clinical matrix teams, escalates emerging safety issues to governance bodies and mentors junior staff within a global matrix environment.