Senior Clinical Trials Operations Leader

Kelly; Greater London; On-site; GBP 40,000 - 60,000; Full time

Job summary

Kelly is looking for a Senior Study Specialist in Greater London. This role involves supporting and leading operational activities for clinical studies with an emphasis on site oversight and vendor management. Essential duties include overseeing CRO activities, managing essential study documents, and training site staff. The ideal candidate has a background in nursing or life sciences and substantial experience in clinical operations, ensuring compliance and quality throughout the study process.

Qualifications

• Bachelor’s degree or higher preferred; relevant industry experience may be considered.
• Experience in biotechnology or pharmaceutical clinical operations.
• Demonstrated experience overseeing external vendors and managing budgets.

Responsibilities

• Support and develop study-specific documentation.
• Manage essential documents across the study lifecycle.
• Oversee CRO activities, including IRB/EC submissions.

Skills

Agility and proactive problem-solving

Leadership and ownership of assigned activities

Strong communication and cross-functional collaboration

Clinical study management and execution

Compliance and quality oversight

Understanding of drug development and study design

Product and therapeutic area knowledge

Education

Bachelor’s degree or higher in nursing, life sciences, or health sciences

Job description

Kelly is looking for a Senior Study Specialist in Greater London. This role involves supporting and leading operational activities for clinical studies with an emphasis on site oversight and vendor management. Essential duties include overseeing CRO activities, managing essential study documents, and training site staff. The ideal candidate has a background in nursing or life sciences and substantial experience in clinical operations, ensuring compliance and quality throughout the study process.