Experienced Trial Talent to Accelerate Your Clinical Studies
In clinical research, time, data integrity, and operational excellence are paramount. Whether you’re managing early-phase studies with novel therapies or overseeing complex global Phase III programmes with established treatments, your success depends on experienced professionals who can lead with rigour, maintain unwavering compliance, and consistently deliver results under pressure.
Axion connects leading life sciences companies with exceptional clinical development and operations talent across all trial phases – from initial feasibility and meticulous site selection through to efficient close-out and robust post-marketing surveillance. Our extensive network spans the UK, DACH, Netherlands, Nordics, and other leading R&D regions, providing you with access to specialists with deep therapeutic area knowledge and global regulatory fluency.
Roles we recruit for
We place experts in
Clinical Project & Programme Management
We deliver strategic leaders to oversee and manage clinical trials, ensuring efficient planning, execution, and delivery.
Clinical Research Associates (CRAs)
We connect you with experienced CRAs to monitor clinical trials, ensuring data integrity and compliance with regulatory guidelines.
Clinical Trial Management & Study Coordination
We provide skilled professionals to manage and coordinate clinical trial activities, ensuring smooth operations and timely completion.
Vendor Oversight & CRO Management
We source experts to effectively manage and oversee vendors and CROs, ensuring quality and efficiency in outsourced clinical research.
Site Monitoring, Start-Up & Close-Out
We deliver specialists to manage site activities, from initiation to close-out, ensuring efficient trial operations.
Clinical Quality & Compliance
We connect you with professionals to ensure adherence to quality standards and regulatory requirements throughout the clinical trial process.
Our candidates ensure:
Phase I–IV experience across a wide range of indications, demonstrating their expertise in diverse clinical settings.
Strong ICH-GCP, EMA, and FDA knowledge, ensuring compliance with global regulatory guidelines.
Operational excellence in timelines, budgets, and site engagement, enabling efficient and cost-effective trial management.
Proven ability to effectively manage complexity and mitigate trial risk, ensuring the success of your clinical programmes.
The Axion Difference
We Specialize by Function, Therapeutic Area, and Geography
Our consultants possess specialised knowledge of clinical development and operations, specific therapeutic areas, and the nuances of various geographic regions, providing you with highly targeted recruitment solutions.
We Access Passive, Highly Experienced Candidates Not Active on the Market:
Our extensive network and proactive search methods allow us to connect you with top-tier clinical professionals who are not actively seeking new roles, giving you access to the best talent in the industry.
We Align Every Placement with Your Trial Needs, Pipeline Milestones, and Compliance Requirements
We go beyond simply filling positions. We take the time to understand your specific trial requirements, pipeline objectives, and compliance obligations, ensuring that every hire is perfectly aligned with your needs.
We Understand How to Support Speed Without Sacrificing Scientific or Regulatory Integrity
We recognise the importance of speed in clinical development, but we also understand the critical need for scientific rigour and regulatory compliance. We provide you with talent solutions that balance efficiency with quality and integrity.
