Clinical Trial Manager

  • Job Reference: 1305 CTM V
  • Date Posted: 30 May 2025
  • Recruiter: Drs Direct Ltd
  • Location: London
  • Salary: £24.59 Per Hour
  • Sector: Occupational Health Nurses
  • Job Type: Temporary
  • Work Hours: Full Time
  • Contact: Victor Ramsay
  • Email: victor@drsdirect.co.uk
  • Telephone: 07427161073

Job Description

This role is a Hybrid role working 21.9hr pw. Interviews will take place anytime throughout May.

Main purpose of the job

An enthusiastic, committed and professional individual is sought for this post. The primary role of the post holder is to set up and support a high quality clinical trial. The post holder will be responsible to a Clinical Project Manager.

Qualifications, experience and knowledge

Degree and/or equivalent experience in Clinical Trials

Experience of managing a clinical trial

Experience of managing a trial of an investigational medicinal product

Comprehensive understanding of UK Clinical Trials Regulations, ICH Good Clinical Practice, the European Directives on Clinical Trials and Good Clinical Practice and the Department of Health’s Research Governance Framework

Experience of monitoring

Evidence of ability to set up and maintain effective management system in trials

Skills and abilities

Evidence of ability to set up and maintain effective management system in trials

Excellent IT skills; MS Office Suite, Trial Databases and other Trial related systems (such as IMP management, Randomisation)

Excellent communication and interpersonal skills

A methodical and accurate approach to work with attention to detail

The ability to make and carry out decisions and know when to confer with colleagues or refer matters onwards

The ability to work without direct supervision; to manage own workload and display good organisational ability

Take responsibility for setting and meeting targets for your own work and others

Desirable Criteria

 

For Grades 7 & 8 include:
Commitment to and knowledge of advancing equality, diversity and inclusion

Experience of using Pharmacovigilance systems

Experience of working in an academic or similar institution

Experience of public speaking and giving presentations

Experience of data management

Ability to evaluate risks inherent in clinical trials and decide those which should be prioritised to ensure that risks are properly managed

Advanced organisational skills, managing several projects that are often time pressured, concurrently

Ability to supervise other members of the team, promote good working relationships and resolve difficult situations

Commitment to and knowledge of advancing equality, diversity and inclusion