Biotechnology Jobs

• 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.

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$242,250 – US$403,750 pa
• Director · manages people

Accountable for end-to-end clinical development strategy for an antibody-drug conjugate asset across multiple tumour types, from first-in-human through registrational trials and launch. Acts as senior clinical representative at governance forums and leads cross-functional, matrixed teams spanning research, precision medicine, medical affairs and commercial.

• Stevenage
• Hybrid · 2 days in office
• US$284,625 – US$474,375 pa
• Director · manages people

Leads clinical development medical activities for cardiovascular and vascular programs across early and later phase studies, shaping clinical development plans, study designs and translational strategies. Provides medical monitoring and safety oversight, leads the clinical matrix team, and engages with regulators, KOLs and cross-functional partners in a hybrid working model.

• Waltham, United States
• Hybrid · 2 days in office
• US$284,625 – US$474,375 pa
• Director · manages people

Leads clinical development medical activities for cardiovascular and vascular programs across early and later phase studies, shaping clinical development plans, study designs and translational strategies. Serves as clinical lead for a matrix team, providing medical monitoring, regulatory input and safety oversight while working with biology, regulatory, commercial and operations colleagues.

• London
• Hybrid · 2 days in office
• US$284,625 – US$474,375 pa
• Director · manages people

Leads clinical development medical activities for cardiovascular and vascular programs across early and late-phase studies, shaping clinical development plans, study designs and translational strategies. Serves as clinical lead for a matrix team, providing medical monitoring, regulatory input and safety oversight while working with biology, regulatory, commercial and operations colleagues.

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$284,625 – US$474,375 pa
• Director · manages people

Leads clinical development medical activities for cardiovascular programs across early and later phase studies, shaping clinical development plans, study designs and translational strategies. Provides medical monitoring and safety oversight, serves as clinical point of contact with regulators and investigators, and leads a cross-functional clinical matrix team within the Cardiovascular Medicine group. Requires a medical degree, board certification in cardiovascular medicine and at least five years of clinical research experience.

• London
• Hybrid · 2–3 days in office
• US$187,275 – US$312,125 pa
• Director

Leads the scientific design and execution of interventional clinical studies within Medical Affairs, providing medical governance, safety data review and scientific oversight of protocols and analysis plans. Collaborates with cross-functional teams, investigators and thought leaders, and presents results for publications and regulatory submissions. Hybrid role with two to three days per week in office.

Digital Tools

• Waltham, United States
• Hybrid · 2–3 days in office
• US$187,275 – US$312,125 pa
• Director

Leads the scientific design and execution of interventional clinical studies within Medical Affairs, providing medical governance, safety data review and scientific oversight of protocols and analysis plans. Collaborates with cross-functional teams, investigators and thought leaders, and presents results for publications and regulatory submissions. Hybrid role with two to three days per week in office.

• USA - Pennsylvania - Upper Providence
• Hybrid · 2–3 days in office
• US$187,275 – US$312,125 pa
• Director

Leads the scientific design and execution of interventional clinical studies within Medical Affairs, providing medical governance, safety oversight and scientific interpretation of protocols and analysis plans. Collaborates with cross-functional teams, investigators and regulators, and presents results for publications and submissions. Hybrid role with two to three days per week in office.

• London
• Hybrid
• US$189,750 – US$316,250 pa
• Director

Leads precision diagnostics strategy for oncology programmes, defining diagnostic requirements for trials and overseeing biomarker selection, assay validation and sample handling. Manages project plans, budgets and timelines while engaging diagnostic companies, clinical labs and vendors, and supporting regulatory submissions. Works cross-functionally with research, clinical, regulatory and commercial teams in a hybrid model.

FDA · EU IVDR · PMDA +2

• Stevenage
• Hybrid
• Director

Leads precision diagnostics strategy for oncology programmes, defining biomarker selection, assay validation and sample collection across multiple assets. Oversees project plans, budgets and regulatory submissions while managing external diagnostic partners and clinical labs. Hybrid role based in Stevenage, relocating to Cambridge by early 2029.

FDA · EU IVDR · PMDA/MHLW Japan +2

• Waltham, United States
• Hybrid
• US$189,750 – US$316,250 pa
• Director

Leads precision diagnostics strategy for oncology programs, defining diagnostic requirements for trials and overseeing biomarker selection, assay validation, and sample collection. Partners cross-functionally with research, clinical, regulatory, and commercial teams, and engages external diagnostic companies and labs to accelerate assay development. Hybrid role based in Waltham, MA.

FDA · EU IVDR · PMDA/MHLW Japan +2

• USA - Pennsylvania - Upper Providence
• Hybrid
• US$189,750 – US$316,250 pa
• Director

Leads precision diagnostics strategy for oncology programmes, defining diagnostic requirements for trials, biomarker selection, assay validation and sample handling. Oversees project plans, budgets and regulatory submissions while managing external diagnostic partners, labs and vendors in a matrixed cross-functional environment.

FDA · EU IVDR · PMDA/MHLW Japan +2

• Waltham, United States
• On-site
• US$150,975 – US$251,625 pa
• Mid-level

Key member of the Clinical Development team contributing to the design, execution, analysis and reporting of clinical studies across all phases. Works cross-functionally with Medical Monitoring, Clinical Operations, Biostatistics, Data Management and Regulatory Affairs, reviewing safety, efficacy, biomarker and PK/PD data and supporting CSRs and regulatory submissions. Based on-site in Waltham, MA or London, UK.

• London
• On-site

Contributes to the design, execution, analysis and reporting of hepatology clinical studies across all development phases, working with clinical operations, biostatistics, data management and regulatory affairs. Reviews safety, efficacy, biomarker and PK/PD data, supports protocol and CSR development, and engages with investigators and sites. Based on-site in London or Waltham, MA.