Project Manager

Entrust Resource Solutions; Aberystwyth; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading resource solutions provider in the United Kingdom is seeking a Project Manager for Clinical & Scientific Support. You will manage clinical trials, assist in compliance, and support project coordination. The ideal candidate has a degree in life sciences, strong organisational and communication skills, and a keen interest in digital health. This is a dynamic role perfect for those who enjoy working across scientific and operational areas.

Qualifications

• Experience in research or project management.
• Strong interest in digital health and regulatory processes.
• Ability to manage multiple tasks effectively.

Responsibilities

• Maintain up-to-date trial documentation and support compliance.
• Assist in preparing study documents and regulatory submissions.
• Conduct literature reviews and stay informed on regulatory updates.
• Provide administrative support to senior managers and help coordinate communications.

Skills

Communication skills

Organisational skills

Technical writing

Digital proficiency

Education

Degree in life sciences

Job description

Project Manager - Clinical & Scientific Support

Initial 12 month Contract

We're looking for a proactive and organised Project Manager to support clinical trials, scientific documentation, and project coordination in a fast‑paced, evolving environment. This role involves managing trial records, supporting compliance, coordinating meetings and travel, and liaising with external partners.

Key Responsibilities:

• Maintain up-to-date trial documentation and support compliance.
• Assist in preparing study documents, scientific publications, and regulatory submissions.
• Conduct literature reviews and stay informed on regulatory updates.
• Provide administrative support to senior managers and help coordinate internal/external communications.

Requirements:

• Degree in life sciences with experience in research or project management.
• Strong interest in digital health, clinical trials, and regulatory processes.
• Excellent communication, organisational, and technical writing skills.
• High digital proficiency and ability to manage multiple tasks effectively.
• A collaborative, solutions-focused mindset.

This role suits someone who thrives in a dynamic setting and enjoys contributing across scientific and operational areas.

To find out more about this opportunity, please contact Lynsey on (phone number removed) or email a copy of your CV to (url removed)