Senior Trials Setup & Compliance Lead – Flexible Hours

Cambscommunityservices; Cambridge; Hybrid; GBP 31,000 - GBP 38,000; Full time

Job summary

A healthcare organization in Cambridge is seeking a Senior Clinical Trials Administrator to manage a portfolio of clinical trials. Responsibilities include overseeing trial setups, ensuring compliance with regulations, and collaborating with research teams. Applicants should have a relevant degree, strong organizational skills, and experience in clinical trial processes. This role offers a flexible work environment, supporting good work-life balance and a wide range of benefits.

Benefits

Development opportunities

On-site leisure facilities

Flexible working arrangements

Qualifications

• In-depth knowledge of setting up cancer clinical trials.
• Experience of data collection within a scientific or medical environment.
• Experience of working autonomously within guidelines.

Responsibilities

• Manage individual trial setup processes from initiation to completion.
• Ensure compliance with local SOPs and regulatory requirements.
• Liaise with study clinicians and research nurses.

Skills

Ability to work in a team

Good communication skills

Good attention to detail

Ability to extract and analyze clinical information

Willing to learn new skills

Education

Educated to degree level or equivalent in relevant subject

Tools

Microsoft Office

Clinical trials database

Job description

A healthcare organization in Cambridge is seeking a Senior Clinical Trials Administrator to manage a portfolio of clinical trials. Responsibilities include overseeing trial setups, ensuring compliance with regulations, and collaborating with research teams. Applicants should have a relevant degree, strong organizational skills, and experience in clinical trial processes. This role offers a flexible work environment, supporting good work-life balance and a wide range of benefits.