Clinical Studies Unit Industrial Placement

Sanofi-aventis Groupe; Reading; On-site; GBP 20,000 - 30,000; Part time

Job summary

A leading pharmaceutical company in the UK seeks a Student Clinical Project Assistant to provide administrative support in clinical trials. As part of the Clinical Studies Unit, you will assist in feasibility studies, prepare reports, and support communication tools. Ideal for students in Biomedical Sciences with strong IT skills. Flexibility and proactivity are key for success in this role.

Qualifications

• Strong IT skills in Word, Excel, PowerPoint, and email.
• Proactive, customer-focused, and able to work both independently and in a team.
• Knowledge of Good Clinical Practice (GCP) is advantageous.

Responsibilities

• Collaborate with medical advisors on feasibility studies.
• Assist in the production of confidentiality agreements.
• Prepare annual and safety reports for ethics committees.

Skills

Strong IT skills in Word, Excel, PowerPoint

Ability to plan and prioritize

Proactive and customer-focused

Flexibility to adapt

Education

Currently in 2nd or 3rd year of a degree in Biomedical Sciences

Job description

Overview

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.

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.

Qualifications

• 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).