Clinical Trial Coordinator
CV-LibraryAbingdon, OxfordshirepermanentPosted: 21 April 2026
Apply NowCure Talent are delighted to be partnered with an established and growing healthcare organisation supporting the delivery of clinical studies across Europe and international markets. As part of their ongoing activity, we are supporting the search for a Clinical Trial Coordinator to join the team and play a key role in study execution and site engagement.
This is a coordination-focused position, supporting multi-centre, multi-country clinical studies. You will work closely with the Clinical Project Manager and cross-functional teams, ensuring studies remain on track, sites are engaged, and data and documentation are maintained to a high standard.
Key Responsibilities
* Track study progress across site activation, recruitment and data entry, ensuring alignment with timelines.
* Act as a key point of contact for investigational sites, supporting day-to-day communication and engagement.
* Support site start-up activities, including document collection and readiness tracking.
* Monitor study metrics, identify risks or delays, and escalate where required.
* Track vendor deliverables and support coordination between external partners, sites and internal teams.
* Maintain and quality check Trial Master File documentation, ensuring completeness and inspection readiness.
* Monitor EDC data entry and query resolution, ensuring consistency with study progress.
* Provide regular updates to the Clinical Project Manager and wider stakeholders.
The Ideal Candidate Will Have
* Proven experience within clinical research, working for a Sponsor or CRO.
* Proven experience supporting multi-centre, multi-country clinical studies.
* Familiarity with GCP and the European clinical research environment.
* Experience working with EDC systems and TMF or eTMF.
* Strong organisational skills, with the ability to manage multiple workstreams and drive follow-ups independently.
* Strong communication skills, with the ability to engage with sites and cross-functional teams.
If you are looking to be part of a collaborative clinical team, supporting the delivery of international studies in a fast-paced environment, get in touch
This is a coordination-focused position, supporting multi-centre, multi-country clinical studies. You will work closely with the Clinical Project Manager and cross-functional teams, ensuring studies remain on track, sites are engaged, and data and documentation are maintained to a high standard.
Key Responsibilities
* Track study progress across site activation, recruitment and data entry, ensuring alignment with timelines.
* Act as a key point of contact for investigational sites, supporting day-to-day communication and engagement.
* Support site start-up activities, including document collection and readiness tracking.
* Monitor study metrics, identify risks or delays, and escalate where required.
* Track vendor deliverables and support coordination between external partners, sites and internal teams.
* Maintain and quality check Trial Master File documentation, ensuring completeness and inspection readiness.
* Monitor EDC data entry and query resolution, ensuring consistency with study progress.
* Provide regular updates to the Clinical Project Manager and wider stakeholders.
The Ideal Candidate Will Have
* Proven experience within clinical research, working for a Sponsor or CRO.
* Proven experience supporting multi-centre, multi-country clinical studies.
* Familiarity with GCP and the European clinical research environment.
* Experience working with EDC systems and TMF or eTMF.
* Strong organisational skills, with the ability to manage multiple workstreams and drive follow-ups independently.
* Strong communication skills, with the ability to engage with sites and cross-functional teams.
If you are looking to be part of a collaborative clinical team, supporting the delivery of international studies in a fast-paced environment, get in touch