Senior Trials Setup & Compliance Lead – Flexible Hours

Transformationunitgm; Cambridge; On-site; GBP 31,000 - GBP 38,000; Full time

Job summary

A leading healthcare organization in Cambridge is seeking an experienced Senior Clinical Trials Administrator. The role involves managing a portfolio of clinical trials, ensuring regulatory compliance, and liaising with study clinicians. Candidates should have a degree in a relevant subject, strong experience in clinical trials, and excellent communication skills. This is a fixed-term position offering flexible working hours. The salary ranges from £31,049 to £37,796 per annum, pro rata.

Benefits

On-site leisure facilities

Reduced cost bus travel

Subsidized parking for eligible staff

Qualifications

• Educated to degree level or equivalent in relevant subject.
• In-depth knowledge of setting up cancer clinical trials.
• Experience in a scientific or medical environment collecting data.

Responsibilities

• Manage portfolios of clinical trials from initiation to completion.
• Liaise with clinicians to ensure regulatory compliance.
• Train other staff members on clinical trial processes.

Skills

Teamwork

Communication skills (telephone, email, face to face)

Attention to detail

Ability to adapt to change

Ability to work under pressure

Education

Degree level or equivalent in relevant subject

Evidence of continuing professional development

Tools

Microsoft Office

Clinical trials database

Job description

A leading healthcare organization in Cambridge is seeking an experienced Senior Clinical Trials Administrator. The role involves managing a portfolio of clinical trials, ensuring regulatory compliance, and liaising with study clinicians. Candidates should have a degree in a relevant subject, strong experience in clinical trials, and excellent communication skills. This is a fixed-term position offering flexible working hours. The salary ranges from £31,049 to £37,796 per annum, pro rata.