28 Research jobs in Cambridge

Deep learning has only just started its transformative impact on the natural sciences. In Microsoft Research AI for Science we are seeking to solve some of the fundamental challenges in the molecular sciences with deep learning.
For our lab in Cambridge, UK or Amsterdam, NL, we are seeking exceptional Machine Learning Research Engineering candidates at the intersection of chemistry and drug discovery. If you are passionate about this research area and believe you can make a lasting impact, we would love to receive your application.
Microsoft's mission is to empower every person and every organization on the planet to achieve more, and we're dedicated to this mission across every aspect of our company. Our culture is centered on embracing a growth mindset and encouraging teams and leaders to bring their best each day. Join us and help shape the future of the world.
This post will be open until the position is filled. When submitting your application, include your CV with a list of publications as an attachment.
**Responsibilities**
+ Drive ML engineering strategy and implementation within an ambitious, high-impact, ML research agenda in the molecular sciences.
+ Design, develop and deploy data processing pipelines, machine learning models and workflows.
+ Work with internal and external partners to deploy and evaluate models and workflows.
+ Champion and coach the team in modern engineering practices.
+ Prepare technical papers and presentations.
+ Work on a day-to-day basis with an international and interdisciplinary research team on one overarching research goal.
**Qualifications**
Required:
+ Strong Experience in Python software development and deployment.
+ Track record in designing, developing and deploying scientific ML systems with real world impact.
+ Experience working with cross-functional teams.
+ Experience working with major cloud platforms and/or HPC.
Preferred:
+ Deep Learning experience.
+ Experience with chemoinformatics & computational chemistry.
+ Experience in real-world drug discovery.
+ Experience with other programming languages.
# Research # AI for Science
Microsoft is an equal opportunity employer. Consistent with applicable law, all qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, color, family or medical care leave, gender identity or expression, genetic information, immigration status, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran or military status, race, ethnicity, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable local laws, regulations and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application process, read more about requesting accommodations ( .

Do you have previous experience with research projects? 

Are you willing to travel on occasions? 

Job Title: Research Administrative Executive

Location: Sawston, Cambridgeshire 

Salary: £25,000

Hours: 37.5 hours

Contract Type: Permanent 

Our client based in Sawston, Cambridgeshire is looking for a Research Administrative Executive.

As a Research Administrative Executive your duties will include:

• Assist with client communication by addressing inquiries and delivering project updates
li>Maintain precise documentation of activities and contribute to quality assurance efforts li>Work alongside internal teams to ensure smooth project execution
• Offer logistical support through scheduling, managing product storage, and coordinating with venues and external interviewers
• Adjust to evolving business demands and work collaboratively with cross-functional teams
• Work in Sawston aswell as occasions in Bury St Edmunds.

An ideal candidate for the Research Administrative Executive

• 1+ years of administration experience
• Good knowledge of MS Excel and MS Word
• Good communication skills, with a willingness to learn and develop professionally.

Ideally you will have experience within a similar position. Interviews will take place in Sawston, Cambridgeshire following a registration process by PureKat Consultancy Ltd. If we have not responded to your application within 3-5 days, unfortunately you have not been successful on this occasion, but please feel free to contact us for other opportunities. PureKat Consultancy is acting as an Employment Agency for permanent vacancies and as an Employment Business for temporary roles.

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher's ( 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System ( which makes everything possible.
The Research Technician - mAbs is responsible for delivering results in developing and evaluating next-gen chromatography media.
This position reports to the Manager Applications & Analytics , and is part of the Fibro R&D department l ocated in Stevenage and will be an on-site role .
What you will do:
+ Responsible for testing and reporting R&D samples for new membrane chromatography products.
+ Write reports and submit data generated from various analytical methods.
+ Provide support to ensure laboratory compliance to Environment Health & Safety regulations
+ Be responsible for executing workload from multiple projects.
Who you are:
+ You will have a Master's degree in a bioscience-based subject
+ You will have at least 1 year of experience using AKTA Pure and/or Pilot systems
+ You will have experience working in a regulated lab
It would be a plus if you also possess previous experience in:
+ Preparing presentations and written reports to support decision-making in multifaceted projects
+ Working in cross-disciplinary teams
+ Use of SEC-HPLC or ProA-HPLC
Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info ( .
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

The Opportunity:

Avantor is looking for a Pathology Research Technician to join our team based in Cambridge. In this role, you'll be responsible for a variety of pathology laboratory activities, including digital slide scanning, tissue sample processing, immunohistochemistry, and quality control of image data, all while ensuring compliance with the Human Tissue Act and Good Laboratory Practice (GLP.

WHJS1_UKTJ

MACHINE LEARNING RESEARCH ENGINEER

• Salary: 48,330 - 62,835
• Location: Cambridge - Triangle/Hybrid (2 days per week in the office)
• Contract: Full Time (35 hours per week), Permanent

Shape the future of AI-powered learning solutions with Cambridge University Press & Assessment, a world-leading academic publisher and assessment organisation, and a proud part of the University of Cambridge.

This is an excitingopportunity for MachineLearning Research Engineers to join our innovative Applied AI team.You'llcontribute to developing, deploying, andmaintainingcutting-edgeAI capabilities that drive the success of Cambridge English's products and services.

About the Role

As a Machine Learning Research Engineer, you will play a pivotal role in driving innovation and advancing AI-powered solutions that enhance Cambridge English products. Your expertise will contribute to the continuous improvement of existing models and the development of cutting-edge technologies that address future business needs.

Key Responsibilities:

• Develop, deploy, and maintain scalable AI-powered solutions for Cambridge English products.
• Optimize and modularize models for reusability and performance.
• Collaborate with product, validation, and business teams to transform capabilities into impactful product features.
• Stay at the forefront of AI and machine learning trends to position Cambridge as a leader in AI-driven assessment and learning.
• Plan, prioritize, and manage own tasks aligned with business objectives.

We are also looking for 2Junior Machine Learning Research Engineers (permanent) and 2Senior Machine Learning Research Engineers (1x permanent, 1x fixed-term). Please visit the linked job postings to apply for these roles.

About You

To thrive in this role, you'll have a passion for AI-driven innovation and the ability to turn ideas into scalable solutions.

Essential Qualifications & Skills:

• Master's degree(or equivalent qualifications and experience)in machine learning or AI/computer science with substantial machine learning component
• Proven hands-on industry experience (minimum 2 years, not including internships) in designing, developing, and deploying machine learning solutions in production environments.
• Advanced programming skills in languages such as Python with a strong focus on code optimization, modular design, and efficiency.
• Deep expertise in developing, training, and deploying models using frameworks like PyTorch and TensorFlow.
• Demonstrated experience in building scalable, production-grade AI services and automated data pipelines with tools like Docker, Kubernetes, and cloud platforms (e.g., AWS).
• Strong understanding of data analysis, model evaluation, and error analysis to drive continuous model improvement.
• Proven ability to collaborate effectively in Agile/Scrum teams and contribute to cross-functional projects.
• Exceptional communication skills for articulating complex technical concepts to both technical and non-technical stakeholders.
• Demonstrated commitment to continuous learning, staying current with state-of-the-art research and applying emerging AI techniques to solve business problems.

Desirable:

• PhD orequivalent qualification and experience in Machine learning or AI/Computer Science
• Experience in applying Natural Language Processing and/or Speech Technology techniques to solve real-world problems.
• Experience applying machine learning to educational assessment and learning solutions.
• Hands-on experience with Large Language Models (LLMs) or foundation models, including fine-tuning and adapting models for specific, production-level applications.

• Contributions to patents or peer-reviewed research publications in machine learning or related AI fields.

Rewards and benefits

We will support you to be at your best in work and to live well outside of it. In addition to competitive salaries, we offer a world-class, flexiblerewards package, featuring family-friendly and planet-friendly benefits including:

• 28 days annual leave plus bank holidays
• Private medical and Permanent Health Insurance
• Discretionary annual bonus
• Group personal pension scheme
• Life assurance up to 4 x annual salary
• Green travel schemes

We are a hybrid working organisation, and we offer a range of flexible working options from day one. We expect most hybrid-working colleagues to spend 40-60% of their time at their dedicated office or location. We will also consider other work arrangements if you wish to work more flexibly or require adjustments due to a disability.

Ready to pursue your potential? Apply now.

We review applications on an ongoing basis, with a closing date for all applications being 28th September, although we may close it earlier if suitable candidates areidentified. Interviews are scheduled to take place as deemed appropriate before or after the closing date.

Please note that successful applicants will be subject to satisfactory background checks including DBS due to working in a regulated industry.

Cambridge University Press & Assessment is an approved UK employer for the sponsorship of eligible roles and applicants under the Skilled Worker visa route. Please refer to thegov websitefor guidance to understand your own eligibility based on the role you are applying for.

MACHINE LEARNING RESEARCH ENGINEER

• Salary: 48,330 - 62,835
• Location: Cambridge - Triangle/Hybrid (2 days per week in the office)
• Contract: Full Time (35 hours per week), Permanent

Shape the future of AI-powered learning solutions with Cambridge University Press & Assessment, a world-leading academic publisher and assessment organisation, and a proud part of the University of Cambridge.

This is an excitingopportunity for MachineLearning Research Engineers to join our innovative Applied AI team.You'llcontribute to developing, deploying, andmaintainingcutting-edgeAI capabilities that drive the success of Cambridge English's products and services.

About the Role

As a Machine Learning Research Engineer, you will play a pivotal role in driving innovation and advancing AI-powered solutions that enhance Cambridge English products. Your expertise will contribute to the continuous improvement of existing models and the development of cutting-edge technologies that address future business needs.

Key Responsibilities:

• Develop, deploy, and maintain scalable AI-powered solutions for Cambridge English products.
• Optimize and modularize models for reusability and performance.
• Collaborate with product, validation, and business teams to transform capabilities into impactful product features.
• Stay at the forefront of AI and machine learning trends to position Cambridge as a leader in AI-driven assessment and learning.
• Plan, prioritize, and manage own tasks aligned with business objectives.

We are also looking for 2Junior Machine Learning Research Engineers (permanent) and 2Senior Machine Learning Research Engineers (1x permanent, 1x fixed-term). Please visit the linked job postings to apply for these roles.

About You

To thrive in this role, you'll have a passion for AI-driven innovation and the ability to turn ideas into scalable solutions.

Essential Qualifications & Skills:

• Master's degree(or equivalent qualifications and experience)in machine learning or AI/computer science with substantial machine learning component
• Proven hands-on industry experience (minimum 2 years, not including internships) in designing, developing, and deploying machine learning solutions in production environments.
• Advanced programming skills in languages such as Python with a strong focus on code optimization, modular design, and efficiency.
• Deep expertise in developing, training, and deploying models using frameworks like PyTorch and TensorFlow.
• Demonstrated experience in building scalable, production-grade AI services and automated data pipelines with tools like Docker, Kubernetes, and cloud platforms (e.g., AWS).
• Strong understanding of data analysis, model evaluation, and error analysis to drive continuous model improvement.
• Proven ability to collaborate effectively in Agile/Scrum teams and contribute to cross-functional projects.
• Exceptional communication skills for articulating complex technical concepts to both technical and non-technical stakeholders.
• Demonstrated commitment to continuous learning, staying current with state-of-the-art research and applying emerging AI techniques to solve business problems.

Desirable:

• PhD orequivalent qualification and experience in Machine learning or AI/Computer Science
• Experience in applying Natural Language Processing and/or Speech Technology techniques to solve real-world problems.
• Experience applying machine learning to educational assessment and learning solutions.
• Hands-on experience with Large Language Models (LLMs) or foundation models, including fine-tuning and adapting models for specific, production-level applications.

• Contributions to patents or peer-reviewed research publications in machine learning or related AI fields.

Rewards and benefits

We will support you to be at your best in work and to live well outside of it. In addition to competitive salaries, we offer a world-class, flexiblerewards package, featuring family-friendly and planet-friendly benefits including:

• 28 days annual leave plus bank holidays
• Private medical and Permanent Health Insurance
• Discretionary annual bonus
• Group personal pension scheme
• Life assurance up to 4 x annual salary
• Green travel schemes

We are a hybrid working organisation, and we offer a range of flexible working options from day one. We expect most hybrid-working colleagues to spend 40-60% of their time at their dedicated office or location. We will also consider other work arrangements if you wish to work more flexibly or require adjustments due to a disability.

Ready to pursue your potential? Apply now.

We review applications on an ongoing basis, with a closing date for all applications being 28th September, although we may close it earlier if suitable candidates areidentified. Interviews are scheduled to take place as deemed appropriate before or after the closing date.

Please note that successful applicants will be subject to satisfactory background checks including DBS due to working in a regulated industry.

Cambridge University Press & Assessment is an approved UK employer for the sponsorship of eligible roles and applicants under the Skilled Worker visa route. Please refer to thegov websitefor guidance to understand your own eligibility based on the role you are applying for.

**Join Us on Our Mission to Drive Healthcare Forward**
As a Clinical Research Associate at IQVIA, you'll play a vital role in advancing clinical research and improving patient outcomes. We're expanding our sponsor-dedicated team and looking for passionate CRAs who are ready to make a difference.
**Why IQVIA?**
+ IQVIA is recognized as #1 in its category on the 2025 Fortune® World's Most Admired Companies list for the FOURTH consecutive year!
+ We offer genuine career development opportunities for those who want to grow as part of the organization.
+ The chance to work on cutting edge medicines at the forefront of new medicines development.
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
**Responsibilities**
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
**Profile**
+ Over 12 months of independent on-site monitoring experience, ensuring compliance with GCP, protocol requirements, and regulatory guidelines.
+ You have successfully managed multiple clinical trial protocols across diverse investigative sites.
+ Flexibility and commitment to nationwide travel
** This role is not eligible for UK Visa Sponsorship**
#LI-AdamThompson
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Join Us on Our Mission to Drive Healthcare Forward**
As a Clinical Research Associate at IQVIA, you'll play a vital role in advancing clinical research and improving patient outcomes. We're expanding our Site Management team and looking for passionate CRAs who are ready to make a difference. This role offers a mix of on-site and remote monitoring, supporting work-life balance while contributing to cutting-edge clinical trials.
**Why IQVIA?**
+ IQVIA is recognized as #1 in its category on the 2025 Fortune® World's Most Admired Companies list for the FOURTH consecutive year!
+ We offer genuine career development opportunities for those who want to grow as part of the organization.
+ The chance to work on cutting edge medicines at the forefront of new medicines development.
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
**Responsibilities**
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
**Profile**
+ Over 12 months of independent on-site monitoring experience, ensuring compliance with GCP, protocol requirements, and regulatory guidelines.
+ You have successfully managed multiple clinical trial protocols across diverse investigative sites.
+ Hands-on experience in the Oncology therapeutic area.
+ Flexibility and commitment to nationwide travel
** This role is not eligible for UK Visa Sponsorship**
#LI-AdamThompson
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Join Us on Our Mission to Drive Healthcare Forward**
As a Clinical Research Associate at IQVIA, you'll play a vital role in advancing clinical research and improving patient outcomes. We're expanding our Site Management team and looking for passionate CRAs who are ready to make a difference. This role offers a mix of on-site and remote monitoring, supporting work-life balance while contributing to cutting-edge clinical trials.
**Why IQVIA?**
+ IQVIA is recognized as #1 in its category on the 2025 Fortune® World's Most Admired Companies list for the FOURTH consecutive year!
+ We offer genuine career development opportunities for those who want to grow as part of the organization.
+ The chance to work on cutting edge medicines at the forefront of new medicines development.
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
**Responsibilities**
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
**Profile**
+ Over 2 years of independent on-site monitoring experience, ensuring compliance with GCP, protocol requirements, and regulatory guidelines.
+ You have successfully managed multiple clinical trial protocols across diverse investigative sites.
+ Hands-on experience in the Oncology therapeutic area.
+ Flexibility and commitment to nationwide travel
** This role is not eligible for UK Visa Sponsorship**
#LI-AdamThompson
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled