Latest Pharmaceuticals Jobs

Associate Director/Director of Statistical Programming

This role involves leading statistical programming activities across clinical programs, ensuring the development and quality control of tables, listings, figures, and analysis datasets. You will oversee external vendors, develop standards and innovative technologies, and support data-driven decision-making in drug discovery.

Recursion United Kingdom £200,600 – £260,200 pa

Remote Permanent

Director, Clinical Pharmacology

This role involves leading the clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs, designing clinical studies, and authoring regulatory documents. You will work closely with cross-functional teams to solve drug development challenges and expedite decision-making through modeling and simulation.

Recursion United Kingdom US$212,900 – US$297,000 pa

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

The Audit Senior Lead role involves performing and managing GMP and compliance audits of biopharmaceutical, vaccine, and pharmaceutical facilities across the EMEA region. Key responsibilities include evaluating compliance, managing stakeholder engagement, and producing clear audit reports to mitigate risks and ensure regulatory adherence.

GSK

On-site Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of biopharmaceutical, vaccine, and pharmaceutical facilities across the GSK Global Supply Chain. You will evaluate compliance with regulatory requirements and provide sterile manufacturing expertise, engaging with senior stakeholders and producing clear audit reports.

GSK

Hybrid Permanent

PV Systems and Processes Lead x2

This role involves maintaining and improving CSL's global pharmacovigilance (PV) system, ensuring compliance with GVP and regulatory requirements. Responsibilities include leading investigations, managing deviations, coordinating inspections, and providing PV training across various functions and affiliates.

CSL United Kingdom

On-site Permanent

Director, Portfolio Development Process & Standards Lead

This role leads the establishment and maintenance of processes and standards across CSL's global Portfolio Development function, ensuring high-quality clinical trial planning, evaluation, and reporting. The Director will drive process improvement, SOP governance, training curriculum development, and cross-functional change initiatives within a dynamic biotech R&D environment. They will work closely with leadership and international teams to reduce complexity, improve quality and speed, and align procedural frameworks across clinical development, biomarkers, and commercial operations.

CSL

Hybrid Permanent

Director – Process Design and Optimisation in Chemical Development

This role involves leading a team in the design and optimisation of chemical processes for drug development. Responsibilities include technical direction, project delivery, regulatory submissions, and mentoring scientists. The position leverages innovative technologies and AI to enhance process efficiency and ensure robust commercial processes.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Logistics Coordinator – Temperature-Controlled Supply (5 Month Secondment

This role involves supporting the day-to-day logistics activities for clinical studies, ensuring medicines are delivered on time and under the correct temperature conditions. You will manage temperature excursions, coordinate with logistics partners, and contribute to continuous improvement initiatives.

AstraZeneca Macclesfield, United Kingdom

On-site Contract

Associate Director, CMC Regulatory Science, International

This role involves developing and implementing CMC regulatory strategies for global submissions, providing guidance on regulatory CMC aspects, and ensuring compliance with health authority guidelines. The candidate will support multiple programs in various therapeutic areas, including vaccines, oncology, and rare diseases, and work closely with manufacturing and quality teams.

Moderna London, United Kingdom

On-site Permanent

Associate Director, CMC Regulatory Affairs, International

This role involves developing and implementing CMC regulatory strategies for international submissions, providing guidance on regulatory CMC aspects, and leading discussions with health authorities. The candidate will also support the creation of CMC submission templates and offer interpretations of regulatory guidance documents, ensuring compliance and efficient delivery of high-quality regulatory documentation.

Moderna London, United Kingdom

On-site Permanent

Clinical Data Analytics Lead

As Clinical Data Analytics Lead, you will transform complex clinical trial data into actionable insights, enhancing decision-making and data quality. You will collaborate with cross-functional teams to drive risk-based approaches, improve study oversight, and support patient outcomes using advanced analytics and visualization tools.

Novartis London, United Kingdom

Hybrid Permanent

Translational Medicine Expert – Dermatology, Associate Director

This role involves leading translational medicine strategies in dermatology, spanning early to late-stage drug development. The expert will drive clinical pharmacology, biomarker development, and regulatory strategies while collaborating across research, development, and external stakeholders. Key responsibilities include study design, safety oversight, and scientific leadership in global project teams.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Business Development Manager (South West)

LOCATION: South West RegionJOB TYPE: Full timeHOURS OF WORK: Monday to Friday, 09:00–17:00 (half hour unpaid lunch break)SALARY: £33,000–£36,000 pa + Uncapped Commission (£45,000 pa OTE) + Car + Benefits.JOB PURPOSEYou will strategically manage a territory of customers, maintaining, developing...

Micronclean Skegness, Lincolnshire, United Kingdom £33,000 – £36,000 pa

Director, Clinical Trial and Data Transparency

This role involves providing strategic and operational expertise for the disclosure of clinical regulatory documents on public websites, ensuring compliance with global regulatory requirements. Responsibilities include managing disclosure activities, overseeing vendors, and developing standard processes and technologic solutions to support transparency in clinical trials.

Pfizer India

Remote Permanent

Director, Clinical Trial and Data Transparency

This role involves leading the strategic and operational aspects of clinical trial transparency and disclosure, ensuring compliance with global regulatory requirements. Responsibilities include managing disclosure activities, overseeing vendors, and developing standard processes for compliance.

Pfizer

Remote Permanent