Clinical Trials Facilitator

2 weeks ago

London, United Kingdom King's College London Full time

Job id: 091085. Salary: £32,979- £36,396 per annum, including London Weighting Allowance.

Posted: 13 June 2024. Closing date: 01 July 2024.

Business unit: Research Management & Innovation. Department: KHP Clinical Trials Office.

Location: Guy’s Campus. Category: Professional & Support Services.

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About us

The King’s Health Partners Clinical Trials Office (KHP-CTO) is a collaboration between King’s College London, Guy’s and St Thomas’ NHS Foundation Trust, King’s College Hospital NHS Foundation Trust and South London and Maudsley NHS Foundation Trust. Established to provide a single interface for those wishing to conduct clinical research within the partner organisations, and to ensure that there are common, efficient processes for the set up and administration of clinical trials.

About the role

Key responsibilities:
Facilitate the collection and preparation of documentation required to confirm local capacity, obtain R&D theme lead approvals, collate regulatory approvals needed to instigate clinical trials

Facilitate the collection of local and regulatory approvals required for the review and implementation of amendments

Provide comprehensive advice to external and internal parties for the conduct of clinical trials across the partner organisations.

To assist in maintaining the records of the clinical trials portfolios of the partner organisations including the EDGE system.

To ensure that trials metrics are collected to permit tracking of milestones.

To assist in the archiving of clinical trials documentation to meet prevailing regulatory requirements.

To maintain a working knowledge of prevailing regulations, guidance, best practices and GCP standards regarding the conduct of clinical trials

To ensure confidentiality of commercially sensitive information and that data protection imperatives are respected

To work closely with Finance and Research Teams to ensure the timely invoicing of commercial trials

The above list of responsibilities may not be exhaustive, and the post holder will be required to undertake such tasks and responsibilities as may reasonably be expected within the scope and grading of the post.

This is a full time post (35 Hours per week), and you will be offered an indefinite contract.

About you

Essential:

- Experience acquired in administration role(s), preferably in either a pharmaceutical industry or clinical research setting
- Strong planning and organisational skills including the ability to prioritize and manage multiple tasks
- Excellent interpersonal skills - tactful and able to deal with a wide range of people in an enthusiastic and helpful manner whilst being capable of firmly maintaining policies and regulations
- Problem solving skills - pragmatic and flexible approach whilst maintaining policies and regulations
- Demonstrably high levels of accuracy and attention to detail
- Demonstrates a proactive approach
- Demonstrates a commitment to a quality culture with a professional demeanour and high ethical standards

Desirable:

- Experience in clinical trial administration and/or in the delivery of clinical research within the NHS
- Knowledge of GCP and full working knowledge of local regulatory requirements for the conduct of clinical trials
- Understanding of Ethics committees and Competent Authority approval processes

Downloading a copy of our Job Description

Full details of the role and the skills, knowledge and experience required can be found in the Job Description document, provided at the bottom of the next page after you click “

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