Latest Medical Affairs Partner - Nephrology & R Jobs

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Interventional Study Scientist Director

This role involves leading the scientific design and execution of interventional clinical studies in oncology or hematology, ensuring high standards of quality and ethics. You will collaborate with cross-functional teams, provide scientific oversight, and engage with healthcare professionals to deliver impactful results.

GSK United Kingdom
On-site Permanent
GSK logo

SERM Scientific Director

The SERM Scientific Director will lead the safety evaluation and risk management of GSK's key assets, ensuring scientifically sound review and interpretation of data. They will develop and execute safety strategies, manage safety governance, and represent GSK on cross-functional teams to address product safety issues and improve regulatory adherence.

GSK
On-site Permanent
Pfizer logo

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and collaboration with internal and external stakeholders.

Pfizer
On-site Permanent
Pfizer logo

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to the study team and investigators.

Pfizer
On-site Permanent
CSL logo

Senior Clinical Trial Case Manager

This role involves leading cross-functional teams in reviewing safety data, mentoring junior staff, and ensuring compliance with GxP guidelines and international regulations. The position also focuses on managing pharmacovigilance procedures, conducting impact assessments of new legislation, and supporting regulatory inspections and audits.

CSL
On-site Permanent
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Director Biostatistics

The Director of Biostatistics leads the statistical aspects of clinical development programs, ensuring robust study design, data analysis, and regulatory submissions. They collaborate closely with cross-functional teams and regulatory authorities to drive the success of clinical trials and therapeutic programs.

CSL
Hybrid Permanent
Isomorphic Labs logo

Technical Program Coordinator, DDMR, London

As a Technical Program Coordinator, you will support the Drug Design and Medical Research (DDMR) function by managing program planning, monitoring timelines, tracking actions, and reporting risks. You will work closely with drug design teams, internal stakeholders, and external partners to ensure effective communication and alignment across the organization.

Isomorphic Labs London, United Kingdom
On-site Permanent
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Supply Planner

The Supply Planner ensures uninterrupted production by managing raw material procurement and inventory across clinical and commercial manufacturing operations. This role involves running MRP processes, maintaining inventory policies, coordinating with suppliers and 3PLs, and leading supply continuity efforts. The position works cross-functionally with finance, quality, and manufacturing teams to align supply plans with demand forecasts and resolve supply chain disruptions.

Autolus Stevenage, United Kingdom
Hybrid Permanent
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Principal Clinical Project Manager

This role leads complex or pivotal clinical trials from conception to closeout, overseeing cross-functional teams and vendor partnerships. The Principal Clinical Project Manager ensures study delivery within quality, timeline, and budget targets, applying risk-based quality management and driving inspection readiness. They also mentor junior staff and contribute to process improvements within clinical operations.

Autolus London, W12 7RH, United Kingdom
Hybrid Permanent
Roche logo

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
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Senior Group Director, Safety Development & Processes

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive...

Roche Welwyn Hatfield, United Kingdom
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Senior Research Scientist

R&D applying AI and algorithms to real-world signals/comms, sensor fusionThis senior position has a three-year term with a leading research institution and has strong Data Science elements. As a PhD-qualified scientist with further research or commercial experience, you will bring...

ECM Selection London, United Kingdom £50,000 – £58,000 pa
Isomorphic Labs logo

Chemistry Lead (Induced Proximity), London

As a Chemistry Lead in the Induced Proximity team, you will develop and apply a cutting-edge platform to tackle traditionally intractable drug discovery problems. You will collaborate with AI/ML and Drug Design teams to drive projects towards clinical trials, focusing on innovative molecular glue design and synthesis.

Isomorphic Labs United Kingdom
Hybrid Permanent
Newton Colmore logo

Senior Bioinformatics Developer - Synthetic Biology

This role involves developing complex bioinformatic algorithms to categorize large datasets, designing sequencing tools, and integrating with lab systems. You will work in a multidisciplinary team of scientists and engineers, leading bioinformatics projects and contributing to cloud-based workflows for research teams.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom
On-site Permanent
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Vice President, Head of Clinical Operations

This role involves leading the clinical operations strategy and execution across Recursion’s full clinical portfolio, from early-stage studies to pivotal trials and submission support. The VP will build scalable operating models, manage global trials, and ensure operational excellence in a data-driven, patient-centered, and technology-enabled environment.

Recursion North Tyneside, NE29 8EP, United Kingdom
On-site Permanent