Latest Research Jobs

Principal Medical Writer

The Principal Medical Writer will lead the creation of high-quality clinical and regulatory documents, working closely with cross-functional teams to ensure scientific rigor and clear communication. This role involves strategic planning, project management, and translating complex data into clear narratives, with a focus on regulatory compliance and process improvement.

GSK United States

On-site Permanent

Principal Medical Writer

The Principal Medical Writer will lead the creation of high-quality clinical and regulatory documents, working closely with cross-functional teams to ensure scientific rigor and compliance. This role involves strategic planning, project management, and translating complex data into clear narratives, with a focus on regulatory submissions and process improvements.

GSK

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory approvals and global market access. The role also includes specialized monitoring, regulatory submissions, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine, working closely with cross-functional teams to design, execute, and interpret clinical studies. Key responsibilities include creating clinical development plans, regulatory submissions, and providing expert input on trial design and execution, while ensuring compliance and strategic insight generation.

Pfizer

On-site Permanent

(Fixed-Term) Manufacturing Associate, Drug Substance - Shift Position

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization,...

Moderna

(Fixed-Term) Manufacturing Associate II - Shift Position

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization...

Moderna

AI Engineer - Intern

As an AI Engineer Intern, you will work on building and optimizing data pipelines for Owkin's agentic AI product, K, which integrates LLMs, tool-calling, and interactive UI elements. You will collaborate with a multidisciplinary team to enhance the user experience, address feedback, and improve the development process through CI/CD workflows and dashboards.

Owkin Paris, France

On-site Internship

Associate Director, Biostatistics (4)

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinicaldevelopment program. The AD provides statistical strategies for the clinical trials and regulatorysubmissions, and is accountable for the statistical deliverables within the program.Lead full scope of...

CSL

VP & Global Head, Discovery Chemistry and DMPK, Oncology Targeted Delivery

This role involves leading the global Discovery Chemistry and DMPK function within AstraZeneca's Oncology Targeted Delivery (OTD) organization. Responsibilities include setting strategic direction, driving innovation in small molecules, ADCs, and RCs, and fostering a high-performing, collaborative culture across R&D sites in Cambridge (UK), Cambridge (MA), and Gaithersburg (US).

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Associate Director, CMC Regulatory Affairs

This role involves leading the development and implementation of CMC regulatory strategies for small molecule drugs in global clinical trials. Responsibilities include managing CMC submissions, providing regulatory guidance, and supporting cross-functional teams in navigating international regulations.

Recursion London, W1C 2QP, United Kingdom £88,200 – £111,100 pa

Hybrid Permanent Flexible

Senior Alliance Manager, London

This role involves managing and nurturing strategic scientific and business partnerships in a cutting-edge AI-driven drug discovery environment. The Senior Alliance Manager will oversee alliance governance, align internal and external teams, and ensure successful delivery of collaborative research and development programs. The position plays a key role in scaling operational frameworks and fostering a collaborative culture across high-impact partnerships.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Principal Data Strategy & Analytics Specialist

This role involves shaping data strategies and leading advanced analytics to support evidence generation and clinical decision-making using real-world and clinical trial data. The specialist will design analytical frameworks, drive data standardization, and collaborate with global teams to integrate complex data sources for patient impact.

Roche Welwyn Hatfield, United Kingdom

Hybrid Permanent

Senior Data Strategy & Analytics Specialist

This role involves designing and executing data strategies that integrate clinical, operational, and real-world data to support drug development. The specialist will act as a subject matter expert in data curation and analytics, working closely with scientific teams to improve data accessibility and usability. The position emphasizes the application of FAIR data principles and production-grade analytical workflows within a regulated environment.

Roche Welwyn Hatfield, United Kingdom

Hybrid Permanent

Data Curator, London

As a Data Curator at Isomorphic Labs, you will work closely with AI experts and drug discovery scientists to curate high-quality, ML-ready datasets. Your role involves integrating large-scale biomedical and biochemical data, enhancing data quality, and collaborating across teams to build and improve data assets that fuel the company's mission to accelerate drug discovery using AI.

Isomorphic Labs London, United Kingdom

On-site Permanent

Associate Director, Biostatistics

The role involves leading statistical strategy and execution across clinical development programs, including study design, data analysis, and regulatory submissions. The individual will provide expert statistical input, manage internal or outsourced programming teams, and represent biostatistics in interactions with global regulatory agencies. Emphasis is placed on innovation, cross-functional collaboration, and delivery of high-quality statistical outputs for clinical trials and submissions.

CSL

Hybrid Permanent