Clinical Trial Administrator — Data Entry & Study Support

THE ROYAL MARSDEN; Belmont; On-site; GBP 21,000 - 32,000; Full time

Job summary

The Royal Marsden invites applications for a Clinical Trial Administrator based at our Sutton site. You will provide essential administrative and data management support across our clinical trial portfolio, entering trial data, resolving queries and maintaining study records.

We value highly organized individuals with excellent communication skills and the ability to manage competing priorities. Cross-site working may be required and experience with GCP is advantageous.

Qualifications

• Proven administrative, database or clinical trial experience.
• Good knowledge of Good Clinical Practice (GCP) advantageous.
• Strong IT skills, particularly Microsoft Excel.
• Excellent attention to detail and communication skills.

Responsibilities

• Enter trial data and resolve queries in the eCRF database.
• Support the Breast Research Governance team with study administration to ensure delivery of trials per GCP and SOPs.
• Assist the Clinical Research Operations Manager with unit administration.
• Liaise with sponsor organisations and R&D departments; act as point of contact for trial sponsors.
• Support monitoring visits and audits and help with archiving.

Skills

Data entry

Query resolution

Attention to detail

Communication

Time management

Excel

Organisation

Tools

eCRF database

Job description

The Royal Marsden invites applications for a Clinical Trial Administrator based at our Sutton site. You will provide essential administrative and data management support across our clinical trial portfolio, entering trial data, resolving queries and maintaining study records.

We value highly organized individuals with excellent communication skills and the ability to manage competing priorities. Cross-site working may be required and experience with GCP is advantageous.