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King's College London

Clinical Trials Associate I

London
£39k – £44k/yr
Posted about 21 hours ago
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About us:

The King’s Health Partners Clinical Trials Office is a collaboration between King’s College London, Guy’s & St Thomas’ NHS Foundation Trust, King’s College Hospital NHS Foundation Trust and South London and Maudsley NHS Foundation Trust. It was set up to provide a single interface for those wishing to conduct clinical trials 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:

The post-holder will conduct clinical trial monitoring activities of clinical trials sponsored or co-sponsored by King’s Health Partners (KHP) Partner Organisations: Guy’s and St Thomas’ NHS Foundation Trust, King’s College Hospital NHS Foundation Trust, and South London and Maudsley NHS Foundation Trust.

  • Ensure adherence to approved protocols and undertake effective source data verification.
  • Ensure that all activities are conducted in accordance with applicable legislation, ICH GCP E6 guidelines, and applicable institutional policies.
  • Working as part of the KHP-CTO Non-Commercial Team, ensure that the sponsor responsibilities (delegated to the KHP-CTO) for clinical oversight, safety reporting, and data integrity are discharged to the highest standards of quality and compliance.

This is a full-time post (35 hours per week) and you will be offered a 14-month contract. We’re looking for someone to start as soon as possible.

About you:

To be successful in this role, we are looking for candidates to have the following skills and experience:

Essential criteria

  • Educated to degree level in a health-related area or equivalent professional experience.
  • Working knowledge of the regulations, guidance and codes of practice pertaining to the conduct of clinical trials in the UK.
  • Able to learn and work to SOPs.
  • Strong planning and organisational skills including the ability to prioritise, manage multiple tasks and projects, with ability to deliver to performance criteria.
  • Strong interpersonal skills, communication skills, influencing skills and problem-solving skills, including the ability to build rapport quickly and collaborate in a cross-functional team.
  • Eye for detail and ability to accurately document findings in written reports.
  • Willingness to travel, including overnight stays.

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Desirable criteria

  • Experience supporting regulatory inspections.
  • Experience of monitoring clinical trials in accordance with GCP (including source data verification).
  • Excellent knowledge of the regulations, guidance and codes of practice pertaining to the conduct of clinical trials in the UK.

Further information:

At King’s, we believe that the diversity of our community and a culture that is welcoming, open, inclusive and collaborative, are great strengths of the university.

The Equality Act of 2010 protects the rights of our students and staff and provides a framework to fulfil our duties to eliminate unlawful discrimination, harassment and victimisation and in addition, to advance equality of opportunity and foster good relations between those who share a protected characteristic and those who do not. At times, this will include balancing rights and beliefs that can feel in tension.

We are committed to free speech and to academic freedom, believing that our foundational purpose as a university, is to create spaces where a wide range of ideas, including ideas that are controversial, can be discussed and debated, and where members of our community can express lawful views without fear of intimidation, harassment or discrimination.

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When engaging in the robust exchange of ideas, we ask that our community is mindful of our Dignity at King’s guidance.

We ask all candidates to submit a copy of their CV, and a supporting statement, detailing how they meet the essential criteria listed in the person specification section of the job description. If we receive a strong field of candidates, we may use the desirable criteria to choose our final shortlist, so please include your evidence against these where possible.

Artificial intelligence (AI) is evolving rapidly, and we recognise its growing role in professional work. Applicants may use AI tools to support preparation of their application, for example to research the role or structure written responses. However, applications must reflect the applicant’s own work and experience. AI tools should not be used during interviews or assessment activities unless this has been agreed in advance as a reasonable adjustment.

We reserve the right to close adverts early due to the volume of applications we receive. While the closing date may change, all adverts will close at 23:59 to allow sufficient time for applications to be submitted on that day.

We encourage you to apply at the earliest opportunity to avoid disappointment as once we have closed a vacancy you will be unable to submit your application.

To find out how our managers will review your application, please take a look at our ‘How we Recruit’ pages.

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Skills

Clinical Trial Monitoring
Source Data Verification
ICH GCP E6 Guidelines
Regulatory Compliance
Planning and Organisation
Interpersonal Communication
Problem-solving
Report Writing
Cross-functional Collaboration
SOP Adherence

Location

London, England, United Kingdom

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