Student Clinical Project Assistant

Sanofi

Reading

Hybrid

GBP 18,000 - 24,000

Part time

3 days ago
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Job summary

Sanofi in Reading, UK is seeking a Student Clinical Project Assistant to support the Clinical Studies Unit. You will assist with feasibility studies, digital innovation projects, and the preparation of ethics submissions while gaining exposure to multiple departments and SOPs.

This 13-month hybrid program offers mentorship and hands-on experience in clinical trial operations, data handling, and communications within a supportive team environment.

Qualifications

  • Currently in 2nd or 3rd year of a degree in Biomedical Sciences or a related field.
  • Strong IT skills in Word, Excel, PowerPoint, and email.
  • Ability to plan, prioritize, and drive results with a strong focus on quality and confidentiality.
  • Proactive, customer-focused, and able to work both independently and collaboratively within a team.
  • Willingness to learn and apply Standard Operating Procedures (SOPs) and quality control processes.
  • Flexibility to adapt to changing priorities and work environments.
  • Knowledge of Good Clinical Practice (GCP) and clinical trial regulations is advantageous but not essential (training provided).

Responsibilities

  • Collaborate with the Cluster Medical Advisor and Site Partnership Managers on feasibility studies in the UK and Ireland, supporting the feasibility process and coordinating responses.
  • Work closely with the local Innovation Lead to support digital innovation initiatives.
  • Assist with the production and maintenance of confidentiality agreements with hospital trusts.
  • Design newsletters and other communication tools to support internal and external communications.
  • Prepare annual and safety reports for submission to ethics committees.
  • Undertake a dedicated project alongside the medical advisors - this year’s focus is on diversity and inclusion in clinical trials.

Skills

Time management
Attention to detail
Communication
Proactive learner

Education

Biomedical Sciences

Tools

Microsoft Excel
Microsoft Word
PowerPoint
Outlook/Email

Job description

Location: Reading, UK

Start date: 15 July 2027

Duration: 13 Months (4 August 2028)

Working Model: Hybrid - 3 days per week

About the job

As a Student Clinical Project Assistant (CPA), you will be part of the Clinical Studies Unit (CSU) at Sanofi. Our unit is responsible for setting up and managing most of the clinical trials conducted by Sanofi in the UK. Your role will primarily focus on providing administrative support to the unit.

You will develop an understanding of the clinical trial process from feasibility through to study close out, working with the CSU Medical Advisors, our Site Partnership Managers and cluster Innovation Lead as well as the clinical study teams. Additionally, you will have opportunities to visit different departments within Sanofi to gain a broader perspective of the company. Ready to grow your skills while helping shape the future of healthcare? At Sanofi, you'll be empowered to learn, ask questions, and bring your ideas to life - all while supported by inspiring mentors and collaborative teams.

Main responsibilities
  • Collaborate with the Cluster Medical Advisor and Site Partnership Managers on feasibility studies in the UK and Ireland, supporting the feasibility process and coordinating responses.
  • Work closely with the local Innovation Lead to support digital innovation initiatives.
  • Assist with the production and maintenance of confidentiality agreements with hospital trusts.
  • Design newsletters and other communication tools to support internal and external communications.
  • Prepare annual and safety reports for submission to ethics committees.
  • Undertake a dedicated project alongside the medical advisors - this year’s focus is on diversity and inclusion in clinical trials.
About you
  • Currently in your 2nd or 3rd year of a degree in Biomedical Sciences or a related field.
  • Strong IT skills in Word, Excel, PowerPoint, and email.
  • Ability to plan, prioritize, and drive results with a strong focus on quality and confidentiality.
  • Proactive, customer-focused, and able to work both independently and collaboratively within a team.
  • Willingness to learn and apply Standard Operating Procedures (SOPs) and quality control processes.
  • Flexibility to adapt to changing priorities and work environments.
  • Knowledge of Good Clinical Practice (GCP) and clinical trial regulations is advantageous but not essential (training provided).
Why choose us?
  • Stretch your skills through apprenticeships, internships, graduate programs, and international experiences that grow with you.
  • Learn from inspiring mentors and collaborative teams while contributing to real projects that shape the future of healthcare.
  • Build your future with access to the latest tools, digital innovation, and continuous learning that keep you ahead of the curve.
  • Grow in a purpose-driven company where your voice matters and your work helps improve millions of lives.
  • Thrive in inclusive, flexible workplaces that support your personal and professional well-being.
  • Launch your career with a company that invests in you - and empowers you to reimagine what’s possible.

We reserve the right to close this vacancy earlier than the advertised closing date should we receive a sufficient number of applications.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

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