Medical Research Project Coordinator
1 week ago
At Pharmiweb, we are seeking a seasoned Clinical Research Associate to join our cFSP team. This role offers an exciting opportunity to work on various medical projects and contribute to the development of innovative treatments.
About the RoleThis position is ideal for professionals with experience in independent on-site monitoring in the UK. As a Clinical Research Associate, you will be responsible for:
- Performing site monitoring visits, including selection, initiation, monitoring, and close-out visits, in accordance with contracted scope and regulatory requirements.
- Collaborating with sites to adapt and drive subject recruitment plans in line with project needs.
- Administering protocol training to assigned sites and establishing regular communication channels.
- Evaluating study site practices related to protocol adherence and escalating quality issues as necessary.
- Managing study progress by tracking regulatory submissions, case report form completion, and data query resolution.
You will also be responsible for ensuring documentation accuracy and maintaining lines of communication with the study team.
RequirementsTo be successful in this role, you should have:
- A life science degree or equivalent industry experience.
- Familiarity with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- The flexibility to travel to sites as required.
We offer a competitive salary of £45,000 - £60,000 per annum, depending on your experience. In addition to your annual salary, you will receive benefits such as:
- Pension scheme contributions.
- Health insurance options.
- A flexible working environment.
IQVIA UK is a leading provider of clinical research services, commercial insights, and healthcare intelligence. Our mission is to create intelligent connections that accelerate the development and commercialization of innovative medical treatments.
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