Skills

Communication Data Analysis Risk Management Quality Assurance Decision-making Research Content Creation Attention to detail Facilitation benchmarking Project Management

Job Specifications

PE Global is currently recruiting for a Clinical Research Scientist/Coordinator for a 12 month contract role with a leading multinational Pharma client based in London.

Primary focus will be supporting the Clinical Design Lab team within the Clinical Science group.

Job Responsibilities

Project Planning, Coordination and Execution: Develop and maintain detailed project timelines, and contribute to 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 escalate as needed. Ensure 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: Creation of 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 optimization.
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.

Requirements

Bachelor’s degree in life sciences, public health, or a related field.
1-2 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 prioritize
Strong attention to detail and highly organized
Successful relationship builder and communicator
Ability to work independently and collaboratively in a fast-paced environment.
Experience with AI tools in clinical development (desirable).

Interested candidates should submit an updated CV.

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***

About the Company

At PE Global, a leading international recruitment agency, we work closely with our candidates to ensure that the opportunities they are considering are the best ones available. PE Global is a resourcing company, with offices in Cork, Dublin, London and India that specializes in offering tailored recruitment solutions to companies and organisations in the domestic and international markets. At PE Global we have been providing cost effective, efficient and customised recruitment services to projects of all sizes since 2005 a... Know more