Clinical Scientist, Early Clinical Development, CVRM

AstraZeneca; Cambridge; On-site; GBP 45,000 - 65,000; Full time

Job summary

A leading global pharmaceuticals company is seeking a Clinical and Translational Scientist in Cambridge, UK. The role focuses on providing scientific support for clinical strategies in metabolic diseases. Candidates should have a Ph.D. and at least 5 years of experience in clinical or translational research. Responsibilities include contributing to trials, preparing regulatory documentation, and liaising with various stakeholders. Opportunities for collaboration on cross-functional teams are available.

Qualifications

• 5+ years of experience in clinical/translational research, particularly in cardiovascular, metabolic, or kidney disease.
• Experience writing clinical synopsis, protocols, and regulatory documents.
• Strong delivery focus and excellent communication skills.

Responsibilities

• Provide scientific support for clinical strategies based on expertise.
• Contribute to pre-clinical and early phase trials.
• Support regulatory documentation and liaise with various departments.

Skills

Clinical or translational research

Biomarker evaluation

Clinical study design

Communication skills

Collaboration on global teams

Education

Ph.D.

Job description

What you’ll do

As a clinical and translational scientist, your core accountability will be scientific support for the scientific and translational science development and execution of clinical strategies based upon your established expertise including the latest thinking about mechanisms of disease, diagnostic approaches, current treatment options, drug development trends, and regulatory requirements in relevant disease and therapeutic areas. You will contribute to pre-clinical and early phase clinical trials and related clinical research projects for potential therapies that are targeting metabolic diseases, as well as serving as an expert on the translational human target validation, clinical design, document generation, conduct, monitoring, data interpretation, and reporting of these studies. Additional tasks include supporting regulatory documentation, liaison with discovery scientists, regulatory, clinical and commercial colleagues, developing and managing external collaborations, and developing a deep knowledge of the literature pertaining to the products under development. You will also work on cross-functional teams within our early clinical development group and across the broader early CVRM organization that are framing our strategies and development plans for potential therapies that are targeting major metabolic disorders, given that these disorders intersect with cardiovascular and kidney diseases and influence disease progression.

Basic Qualifications

• Ph.D with minimum of 5 years of experience in clinical or translational research in cardiovascular, metabolic, or kidney disease
• Experience in biomarker evaluation, human target validation, or translational science knowledge
• Proven experience in writing clinical synopsis/protocols, regulatory materials and clinical study supporting documents
• Experience in assisting in the design and execution of clinical studies as well as researching patient characteristics, treatments and care
• Demonstratable clinical scientific knowledge in either cardiovascular, metabolism and/or kidney disease
• Good publication track record
• Track record of strong delivery focus, excellent communication skills and ability to collaborate successfully on global cross-disciplinary teams

Preferred Qualifications

• Advanced Masters or doctoral degrees
• Experience working in an early clinical trial/research setting within the pharmaceutical industry including preparation of documents supporting clinical trials.

Location: Office based in Cambridge, UK

Are you ready to bring new insights and fresh thinking to the table? Good, because we can’t wait to hear from you.

Date Posted: 30-Oct-2025

Closing Date: [see organizational posting]

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.