Clinical Project Assistant

SRG; England; On-site; GBP 35,000 - 50,000; Full time

Job summary

A leading consulting company is seeking a Project Associate to support clinical development initiatives in the London Area. This role requires experience in project management and clinical research, along with a Bachelor's degree in life sciences or a related field. The ideal candidate will have strong organizational and communication skills, proficiency in Microsoft Office, and the ability to work in a fast-paced environment. This position offers contract employment within a dynamic team.

Qualifications

• 2-3 years of experience in clinical research, project coordination, or consultancy.
• Understanding of drug development processes and clinical trial regulations.
• Proficiency in Microsoft Office and project management tools.

Responsibilities

• Support planning and execution of clinical development initiatives.
• Maintain project timelines and ensure effective communication.
• Monitor project deliverables for quality assurance.

Skills

Project management

Organizational skills

Communication skills

Data analysis

Stakeholder management

Education

Bachelor’s degree in life sciences, public health, or related field

Tools

Microsoft Office

Project management tools

Job description

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To be successful in this role, candidates must have strategic, cross-functional project management experience and prior exposure to change management within the pharmaceutical industry. Additionally, at least 2 years of management consulting experience along with a solid understanding of clinical development, are essential.

Job Purpose

The Project Associate (PA) supports the planning and execution of multiple clinical development initiatives. Working closely with Clinical Development colleagues and cross‑functional stakeholders, the PA drives operational efficiency and contributes to successful project delivery. The role ensures project activities are well‑organized, deadlines are met, and communication flows effectively.

Major Activities

• Project Planning, Coordination and Execution: Develop and maintain detailed project timelines and contribute to the content of key deliverables. Ensure all aspects of the project are organized and tracked effectively. Monitor completion status of deliverables, flag issues and opportunities, and elevate as needed. Ensure the team is working in alignment with project objectives. Maintain project dashboards and support reporting for governance reviews.
• Documentation Management: Maintain and manage project documents, reports, and meeting agendas/minutes, ensuring that all records are accurate and accessible.
• Meeting Preparation & Facilitation: Schedule, prepare, and co‑facilitate project meetings and workshops, ensuring adherence to meeting excellence standards (agenda, minutes, action items).
• Communication: Act as a liaison between project teams and stakeholders, facilitating seamless information flow and collaboration.
• Content creation: Create structured content in PowerPoint to support project needs and communication with project teams and stakeholders.
• Quality Assurance: Monitor project deliverables to ensure they meet predefined quality standards. Contribute to continuous improvement initiatives and process optimisation.
• Risk Management: Identify potential risks in project execution and collaborate with the team to develop strategies to mitigate these risks.
• Data Analysis: Analyze project‑related data to extract insights that support informed decision‑making. Contribute to benchmarking and background research on regulatory landscapes and industry practices.

Primary focus will be supporting the Protocol Design Excellence (PDE) team within the Clinical Science group.

Education and Professional Experience

• Bachelor’s degree in life sciences, public health, or a related field.

Languages

• Fluent English (oral and written)

Experience / Professional Requirements

• 2‑3 years of experience in clinical research, project coordination, or consultancy.
• Understanding of drug development processes and familiarity with clinical trial processes and regulatory frameworks.
• Strong organisational, project management and communication skills.
• Proficiency in Microsoft Office and project management tools.
• Delivery focus; reliable and respond promptly to requests.
• Ability to multi‑task and prioritise.
• Strong attention to detail and highly organized.
• Successful relationship builder and communicator.
• Ability to work independently and collaboratively in a fast‑paced environment.
• Desirable: Experience with AI tools in clinical development.

Seniority level

Associate

Employment type

Contract

Job function

General Business, Pharmaceutical Manufacturing

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