Biotechnology Jobs

• Cambridge
• Hybrid · 3 days in office
• Director

Lead digital health strategy engagements with AstraZeneca R&D, top pharma and biotechs, shaping operating models and roadmaps across clinical development. Directs project teams on AI and digital solutions such as ePRO/eCOA, wearables and digital biomarkers, building business cases and tracking value realisation. Combines consulting, protocol design support and scaled implementation in a matrixed environment.

ePRO · eCOA · Wearables +1

• Waltham, United States
• Hybrid · 2 days in office
• US$189,750 – US$316,250 pa
• Director · manages people

Provides clinical and scientific leadership across early-phase clinical development programs in GSK's Respiratory, Immunology & Inflammation Research Unit, focusing on aging. Leads the Clinical Matrix Team, designs clinical development plans and study protocols, oversees medical monitoring and safety, and represents programs in regulatory interactions. Works cross-functionally with biology, translational sciences, commercial, and regulatory partners.

• Stevenage
• Hybrid · 2 days in office
• US$189,750 – US$316,250 pa
• Director · manages people

Provides clinical and scientific leadership across translational and clinical studies within GSK's Respiratory, Immunology & Inflammation Research Unit, with a focus on aging. Leads a Clinical Matrix Team, designs clinical development plans and protocols, and oversees medical monitoring, safety and regulatory interactions. Hybrid working with at least two days per week on-site, initially in Stevenage before a planned relocation to Cambridge, UK.

• London
• Hybrid
• Director

Lead global regulatory strategy for renal therapy programs across all development phases, serving as the regulatory representative on cross-functional teams. Drive major submissions such as INDs, NDAs, BLAs and MAAs, and lead health authority interactions, while mentoring regulatory team members. Distinct for its international scope and focus on renal, nephrology and rare disease assets.

IND · CTA · NDA +2

• London
• Hybrid
• Director · manages people

Leads global operational delivery of early development oncology programs, managing Clinical Project Managers, Monitoring Leads and CTAs. Owns the clinical development plan, CRO and site selection strategy, budgets and timelines, and serves on Asset Teams. Requires deep first-in-human and Phase I oncology trial expertise.

Microsoft Office

• Reading
• Remote
• Lead

Provides strategic medical and scientific subject matter expertise in hematology-oncology, advising internal stakeholders on protocol design, clinical development plans and proposals, and supporting client bid-defense meetings. Acts as an internal and external consultant across the research and development lifecycle, coaching project teams and collaborating with business development and operations. Greater independence is expected over time under the therapeutic area head.

• 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

• Uxbridge
• Director · manages people

Owns the clinical strategy for one or more neuropsychiatry programs, serving as Clinical Trial Physician and clinical point of accountability for the Clinical Development Team. Leads trial design, data interpretation, regulatory submissions and health authority interactions, with matrix leadership across global scientific teams.

• Uxbridge
• Director · manages people

Leads clinical strategy and execution for one or more GI oncology indications of a given asset, owning the Target Product Profile and disease area strategy. Manages a team of physicians and scientists designing, running, analysing and interpreting all clinical studies, and acts as internal and external clinical authority for regulatory interactions and business development. Requires deep therapeutic expertise and 8+ years of drug development experience, with international and domestic travel.

• Remote Opportunity - United Kingdom
• Remote
• £136,500 – £167,200 pa
• Director

Lead clinical pharmacology and pharmacometrics strategy across a portfolio of rare disease and oncology programs, serving as the clinical pharmacology lead for regulatory interactions and study design from Phase 1-3. Perform and oversee modeling and simulation with tools such as WinNonlin, Monolix, NONMEM and R, and author regulatory sections for IBs, INDs and NDAs. Part of a Pharmacometrics team spanning clinical pharmacology, pharmacometrics and translational modeling, working end-to-end across discovery and development.

WinNonlin · Monolix · NONMEM +1

• Remote Opportunity - United States
• Remote
• US$261,800 – US$346,060 pa
• Director

Lead clinical pharmacology and pharmacometrics strategy across a portfolio of rare disease and oncology programs, serving as the clinical pharmacology lead and regulatory representative. Oversee modeling and simulation (population PK, PK-PD, exposure-response) and provide pharmacology input on Phase 1-3 study designs. Work cross-functionally with clinical, translational and discovery teams in an end-to-end drug development environment.

WinNonlin · Monolix · NONMEM +1

• Leeds
• Director · manages people

Executive leadership role owning QA and regulatory compliance for the Clinical Pharmacology Services unit, covering CPU operations, GMP pharmacy activities and Phase IB/IIA early-phase trials. Sets risk-based quality strategy, inspection readiness and audit programs, leads global matrixed QA teams and represents the company externally on GCP/GMP matters.

• Maidenhead
• Hybrid · 3 days in office
• US$317,000 – US$409,000 pa
• Director · manages people

Leads a cross-functional Clinical Development Team as the lead scientific expert, owning the clinical strategy, plan and medical monitoring for immunoglobulin programs. Accountable for clinical content of regulatory submissions and study documents, and serves as medical monitor across trials in a matrixed environment.

• Opfikon, Switzerland
• Hybrid · 3 days in office
• US$317,000 – US$409,000 pa
• Director · manages people

Leads the cross-functional Clinical Development Team as lead scientific expert, owning the Clinical Development Plan and integrating internal and external contributions into program strategy. Serves as medical monitor, authors key regulatory and study documents, and presents to safety and review committees.

• Oxford
• Hybrid · 3–4 days in office
• Director

As an individual contributor in the Clinical Pharmacology group, you will develop quantitative strategies for dose selection, PK/PD characterization and regimen optimization across oncology, immunology and rare disease programs. You will partner with Pharmacometrics and QSP colleagues, represent CQP on program teams, and contribute to regulatory documentation and interactions.

R · Phoenix WinNonlin · NONMEM +2