Jobs in Cambridge

Director, Translational Medicine, Oncology, Cambridge, MA

Lead the development and execution of translational medicine strategies for oncology programs, integrating AI-driven insights to inform clinical trial design and biomarker development. Collaborate with cross-functional teams to translate preclinical findings into clinical applications and advance companion diagnostics. Play a key role in shaping the scientific direction of early-stage drug development using cutting-edge methodologies and digital biology approaches.

Isomorphic Labs Cambridge, United Kingdom

Principal Medical Writer

Author and deliver high-quality clinical regulatory documents such as protocols, Clinical Study Reports (CSRs), and Investigator’s Brochures. Lead the development of clinical dossier submissions, interpret complex clinical and statistical data, and collaborate with cross-functional teams to ensure regulatory compliance and timely delivery. Work within a hybrid model, balancing remote and in-office settings, while supporting global submissions across key therapeutic areas.

GSK CA$118,000 – CA$168,000 pa

Head of RTSM (Randomization and Trial Supply Management)

Lead the RTSM function for clinical trials, designing and delivering patient-focused randomization and trial supply strategies across Phase I–IV programs. Partner with cross-functional teams and vendors to ensure reliable supply and randomization systems, while building team capability and driving process improvements aligned with clinical development and regulatory standards.

GSK €119,250 – €198,750 pa

12 Month University Industrial Placement Student (UIPS): Analytical Chemistry

This 12-month industrial placement involves supporting the development of pharmaceutical drugs through analytical chemistry techniques such as HPLC, GC-MS, NMR, and XRPD. You'll work within a collaborative team to deliver analytical data that supports drug development timelines, adhering to GMP and GLP standards while gaining hands-on experience in a regulated environment.

AstraZeneca Cambridge, United Kingdom £28,000 pa

12 Month University Industrial Placement Student (UIPS): Synthetic - Organic Chemistry

This 12-month industrial placement offers hands-on experience in synthetic organic chemistry within a pharmaceutical R&D environment. You'll work alongside experienced chemists to design and develop novel synthetic routes for potential drug candidates, using techniques such as purification, reaction monitoring, and automation. The role provides exposure to either medicinal/peptide chemistry in Cambridge or process development in Macclesfield, with opportunities to present work and build key scientific and communication skills.

AstraZeneca Macclesfield, United Kingdom £28,000 pa

Principle Scientist - Cheminformatics

This role involves developing and deploying advanced computational and machine learning models to accelerate drug discovery within GSK's BRADSHAW platform. The Principal Scientist will integrate cheminformatics, quantum mechanics, and AI-driven workflows to support decision-making across discovery programmes. Emphasis is placed on collaboration with multidisciplinary teams and translating complex data into actionable insights for non-experts.

GSK Stevenage, United Kingdom

Regulatory Affairs Manager, Oncology Therapeutic Group, Global Regulatory Affairs

This role involves developing and executing global and regional regulatory strategies for oncology products across their lifecycle, ensuring compliance and optimal labeling. The manager will collaborate with cross-functional teams and regulatory authorities to support submissions and approvals, leveraging regulatory intelligence to inform decision-making. The position emphasizes strategic planning, stakeholder engagement, and innovation within a patient-focused biopharma environment.

GSK Stevenage, United Kingdom

Hybrid Permanent

Safety Scientist – SERM (Safety Evaluation and Risk Management)

A Safety Scientist in GSK's Safety Evaluation and Risk Management (SERM) team leads signal detection, safety evaluations, and risk management for pharmaceutical products in clinical development and post-marketing. The role involves authoring safety reports, contributing to Risk Management Plans, and collaborating across global teams to ensure patient safety. The position supports governance activities and requires strong scientific, medical, and pharmacovigilance expertise.

GSK Irvine, Alba / Scotland, KA12 8EL, United Kingdom PLN 215,250 – PLN 358,750 pa

Safety Scientist – SERM (Safety Evaluation and Risk Management)

This role involves leading safety evaluation and risk management for GSK’s global pharmaceutical products, both in clinical development and post-marketing settings. The Safety Scientist will conduct signal detection, contribute to Risk Management Plans, author safety reports, and collaborate across functions to ensure patient safety. The position requires scientific rigor, regulatory knowledge, and strong cross-functional leadership in a hybrid working environment.

GSK Stevenage, United Kingdom PLN 215,250 – PLN 358,750 pa

Safety Scientist – SERM (Safety Evaluation and Risk Management)

This role involves leading safety evaluation and risk management activities for GSK’s global pharmaceutical products, both in clinical development and post-marketing settings. The scientist will conduct signal detection, author safety reports, contribute to risk management plans, and collaborate across functions to ensure patient safety. The position emphasizes scientific rigor, regulatory compliance, and cross-functional leadership within a global team environment.

GSK Worthing, United Kingdom PLN 215,250 – PLN 358,750 pa

12 Month University Industrial Placement Student (UIPS): Synthetic - Organic Chemistry

This 12-month industrial placement offers hands-on experience in synthetic organic chemistry within AstraZeneca’s drug discovery and development teams. Placement students in Cambridge will work on novel multi-step syntheses with medicinal or peptide chemists, while those in Macclesfield will focus on scalable, sustainable process chemistry for kilogram-scale production. The role involves techniques in organic synthesis, purification, automation, and cross-team collaboration, with opportunities to present work and build transferable scientific skills.

AstraZeneca Cambridge, United Kingdom £28,000 pa

Safety Scientist – SERM (Safety Evaluation and Risk Management)

This role involves leading safety evaluation and risk management for GSK’s pharmaceutical products, focusing on signal detection, safety reporting, and risk mitigation across clinical and post-marketing stages. The scientist will collaborate with cross-functional teams, contribute to global regulatory submissions, and ensure patient safety through rigorous data analysis and scientific interpretation. Work is conducted in a hybrid model with an eventual move to Cambridge.

GSK Barnard Castle, United Kingdom PLN 215,250 – PLN 358,750 pa

Regulatory Affairs Manager, Oncology Therapeutic Group, Global Regulatory Affairs

Develop and execute global regulatory strategies for oncology assets, ensuring compliance and optimal labeling across markets. Collaborate with cross-functional teams and regulatory authorities to support product development and approvals. Drive innovation and process improvements within the regulatory lifecycle.

GSK United Kingdom €98,250 – €163,750 pa

Regulatory Affairs Manager, Oncology Therapeutic Group, Global Regulatory Affairs

Develop and execute global regulatory strategies for oncology assets, ensuring compliance and optimal labeling across regions. Collaborate with cross-functional teams to align regulatory plans with development goals and support submissions to health authorities. Focus on innovation, patient impact, and navigating complex regulatory landscapes in a hybrid working environment.

GSK €98,250 – €163,750 pa

Regulatory Affairs Manager, Oncology Therapeutic Group, Global Regulatory Affairs

Develop and execute global regulatory strategies for oncology assets, ensuring compliance and optimal product labeling across regions. Collaborate with cross-functional teams and regulatory authorities to support product development and approvals. Drive innovation and process improvements within the regulatory lifecycle.

GSK €98,250 – €163,750 pa