Clinical Trial Expert

Role: Clinical Trial Expert
Location: Welwyn
Hours: Monday - Friday
Pay: 301.57 - 339.57 per day (PAYE) OR 400.00 - 450.00 per day (UMB)
12 Month Contract Inside of IR35

An excellent opportunity has arisen for a Clinical Trial Expert to join one of our longstanding clients, an exciting global client in Welwyn.

Benefits:

• Hybrid (2 days in office), providing flexibility when able
• Weekly competitive pay.
• Free parking onsite
• 25 days holiday per annum + recognised bank holidays
• Opportunity to work in a dynamic and diverse organisation.
• Exposure to cutting-edge clinical trial innovations.
• Professional growth and development opportunities.

The Requirements:

• Experience in pharmaceutical or healthcare industries with knowledge of drug development processes.
• University degree (Life Sciences preferred) or equivalent experience.
• Strong background in clinical trial execution, including understanding of ICH-GCP and regulatory requirements.
• Expertise in clinical trial management tools such as IxRS, eCOA, and digital biomarkers.
• Strong leadership, collaboration, and problem-solving skills.
• Ability to navigate fast paced and ambiguous environments while maintaining attention to detail.
• Experience in project management and process improvement methodologies.
• Willingness to travel internationally as required.

The Role:

As a Clinical Trial Expert, you will be responsible for executing clinical trials across all phases, ensuring operational excellence, and driving productivity. Key responsibilities include:

• Supporting trial execution strategies and contributing to study design.
• Establishing and maintaining relationships with internal and external stakeholders.
• Ensuring compliance with regulatory requirements and participating in audits and inspection readiness.
• Managing systems and tools essential for trial operations, including eCOA and IxRS.
• Coordinating study start-up components such as imaging and investigator training.
• Developing and maintaining trial oversight documentation (e.g., risk management plans, monitoring plans).
• Tracking study progress and collaborating with teams to resolve challenges.
• Driving efficiency across clinical operations by standardising processes and supporting portfolio-wide initiatives.

If you're keen to join an exceptional team who can offer an excellent working environment and opportunities, then please apply to this Clinical Trial Expert role below or call Chloe McCausland on (phone number removed) between 9:00am and 5:00pm.