Clinical research Work, Jobs in Comberton, Cam (with Salaries)

Clinical Research Associate
AstraZeneca —Cambridge
- Bachelor's degree
- No degree
- Travel
1d
Project Coordinator
Activinsights Ltd —Huntingdon
- £28,000 - £30,000 a year
- Full-time
- Microsoft Excel
- Microsoft Office
- Organisational skills
- Free parking
- Life insurance
Quick apply
12d
Clinical Trial Coordinator
Thermo Fisher Scientific —Cambridge
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- English
Clinical Research Nurse - GP Surgery based
St Mary's Surgery —Ely
- Part-time
Quick apply
2d
Clinical Research Associate
TOGL (Holdings) Limited —Cambridge
- Patient monitoring
- In-person
- Communication skills
Quick apply
5d
Laboratory Technician in Molecular Diagnostics for Colorectal Cancer Screening
TOGL (Holdings) Limited —Cambridge
- Full-time
- Bachelor's degree
- Organisational skills
- Communication skills
Quick apply
12d
Research Governance Assistant
Cambridgeshire and Peterborough NHS Foundation Trust —Cambridge
- £32,073 - £39,043 a year
- Full-time
- Patient care
4d
Clinical Trial Coordinator/Clinical Research Nurse
Royal Papworth Hospital NHS Foundation Trust —Cambridge
- £32,073 - £39,043 a year
- Full-time
- IT
- Communication skills
Laboratory Operations Assistant
TOGL (Holdings) Limited —Cambridge
- Full-time
- Laboratory experience
- English
- Data entry
- Annual leave
Quick apply
1d
Scientist I/II, Formulation Development
Abzena Inc. —Cambridge
- £27,000 - £33,000 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- Laboratory experience
Quick apply
2d
Senior Scientist in Molecular Diagnostics for Colorectal Cancer Screening
TOGL (Holdings) Limited —Cambridge
- Full-time
- Doctoral degree
- Laboratory experience
- Master's degree
Quick apply
12d
Senior Research Associate, Discovery & Engineering (On-site: Cambridge, UK)
FairJourney Biologics —Cambridge
- £32,000 - £38,000 a year
- Full-time
- Data analysis skills
- Laboratory experience
- Master's degree
- Life insurance
Quick apply
Clinical Research Fellow in Psychiatry
Cambridgeshire and Peterborough NHS Foundation Trust —Cambridge
- £54,499 - £67,325 a year
- Full-time
4d
Lead Pharmacist for Clinical Trials, Research, and Innovation
Royal Papworth Hospital NHS Foundation Trust —Cambridge
- £57,528 - £64,750 a year
- Full-time
- Master's degree
- Communication skills
- Hospital experience
10d
Global Scientific Lead - Clinical Outcome Assessment (COA) Strategy Consulting - Multiple locations - Hybrid/Home-based
IQVIA —Cambridge
- Hybrid work
- Management
- Doctoral degree
- English
Clinical Study Manager
Qureight Ltd —Cambridge
- Full-time
- Hybrid work
- Project management
- Machine learning
- Annual leave
- Life insurance
Quick apply
Director, Project Team Lead, Early Research
Flagship Pioneering, Inc. —Cambridge
- Doctoral degree
- Laboratory experience
- Master's degree
Team Leader - Biostatistics
Bio Pharma Resourcing —Cambridge
- £35,000 - £50,000 a year
- Management
- Doctoral degree
- Master's degree
Sector Manager- Immunoassay
Resolian —Fordham
- Full-time
Computational Biologist
Cyted Health —Cambridge
- £45,000 - £60,000 a year
- Full-time
- Doctoral degree
- Master's degree
- University
- Life insurance

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Clinical Research Associate

AstraZeneca -
Cambridge

Apply Now

Job details

1 day ago

Qualifications

Bachelor's degree
Communication skills
Negotiation

Full job description

Location Cambridge, England, United Kingdom Job ID R-255019 Date posted 02/07/2026

Job Title: Clinical Research Associate

Location: UK - Field-based,

Introduction to role:

As a Clinical Research Associate, you will be the primary face of our studies at assigned sites, ensuring excellence from start-up through close-out. You will collaborate closely with local study leadership and cross-functional partners to uphold the highest standards of quality, compliance and patient safety. Your work will directly influence trial timelines, data integrity and the speed at which new therapies move forward.

In this role, you will bring structure and momentum to complex studies training and guiding site teams, leveraging risk-based approaches, and translating insights from the field into action. You will join a community that pairs scientific rigor with digital and data driven tools, all in service of delivering life-changing medicines to people who need them most.

Accountabilities:

Contribute to identifying and assessing potential investigators to build a high-performing site network aligned with protocol needs and patient access.
lead start-up and regulatory maintenance including Site Qualification Visits; collection, preparation, review and tracking of documents; and submissions to EC/IRB and Regulatory Authorities for study start-up and throughout the study.
Train, support and advise Investigators and site staff on study-specific requirements and Risk Based Quality Management principles; confirm completion and documentation of required training, including ICH-GCP; keep sites inspection-ready at all times.
Actively participate in Local Study Team meetings and contribute to National Investigators meetings as applicable; share recruitment and site performance insights to drive data-informed decisions and actions.
Initiate, monitor and close study sites in line with AstraZeneca Procedural Documents and the study-specific Monitoring Plan; perform remote and onsite visits and remote data checks; collaborate with LSAD on visit timing and type when required.
Perform Source Data Review, Case Report Form review and Source Data Verification per the Monitoring Plan; conduct regular Site Quality Risk Assessments and adapt monitoring intensity accordingly; ensure timely data query resolution and partner with data management to drive robust data quality.
Ensure accurate and timely reporting of Serious Adverse Events and follow-ups; escalate systematic or serious quality issues, data privacy breaches and CSP or ICH-GCP compliance issues per local processes; ensure compliance with the Code of Ethics, company policies (including SHE) and local/national/regional legislation.
Manage study supplies, drug supplies and drug accountability at sites; prepare study drug for destruction where applicable.
Update CTMS and other systems within required timelines; prepare and finalize monitoring visit reports and follow-up letters in line with SOPs; ensure timely collection and upload of essential documents into the eTMF and support regular QC checks; ensure site documents and communications are ready for archiving and completion of the local eTMF.
Prepare for and collaborate during audits and regulatory inspections with LSAD and CQAD; assist sites in maintaining an inspection-ready ISF.
Provide feedback on research-related information including site and investigator insights and competing studies; collaborate with local MSLs as directed by LSAD or line manager.
Drive site performance by proactively identifying issues, resolving them promptly and escalating appropriately; with tenure and experience, take on additional responsibilities associated with LSAD to broaden your impact.

Essential Skills/Experience:

Bachelor degree in related discipline, preferably in life science, or equivalent qualification.
Excellent knowledge of international guidelines ICH-GCP
Good knowledge of relevant local regulations.
Good knowledge and experience of cell and gene therapies
Understanding of the drug development process.
Prior experience in monitoring clinical trials in late phases ( 2-4), study drug handling and data management.
Excellent attention to details.
Good written and verbal communication skills.
Good collaboration and interpersonal skills. Good negotiation skills.
Ability to travel nationally/internationally as required.

Desirable Skills/Experience:

Ability to work in an environment of remote collaborators.
Manages change with a positive approach for self, team and the business; sees change as an opportunity to improve performance and add value.
Ability to champion more efficient and effective methods and processes to deliver quality clinical trials with reduced budget and in less time.
Good analytical and problem-solving skills.
Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines.
Familiarity with risk-based monitoring approaches, including remote monitoring.

What is next:

Take the next step and turn your monitoring expertise into real-world patient impact join us to deliver smarter, faster trials.

We look forward to receiving your application not later than 12th July 2026.

Date Posted

03-Jul-2026

Closing Date

12-Jul-2026

Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.

Apply Now

Refine Your Search

clinical research jobs in comberton, cam

Clinical Research Associate

Project Coordinator

Clinical Trial Coordinator

Clinical Research Nurse - GP Surgery based

Clinical Research Associate

Laboratory Technician in Molecular Diagnostics for Colorectal Cancer Screening

Research Governance Assistant

Clinical Trial Coordinator/Clinical Research Nurse

Laboratory Operations Assistant

Scientist I/II, Formulation Development

Senior Scientist in Molecular Diagnostics for Colorectal Cancer Screening

Senior Research Associate, Discovery & Engineering (On-site: Cambridge, UK)

Clinical Research Fellow in Psychiatry

Lead Pharmacist for Clinical Trials, Research, and Innovation

Global Scientific Lead - Clinical Outcome Assessment (COA) Strategy Consulting - Multiple locations - Hybrid/Home-based

Clinical Study Manager

Director, Project Team Lead, Early Research

Team Leader - Biostatistics

Sector Manager- Immunoassay

Computational Biologist

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