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Senior clinical field specialist

Peterborough
JR United Kingdom
Posted: 28 June
Offer description

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Senior Clinical Field Specialist, Peterborough

Client:

The Mullings Group

Location:

Peterborough, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

Job Views:

6

Posted:

26.06.2025

Expiry Date:

10.08.2025


Job Description:

In recent decades, treatment of heart attacks by minimally invasive percutaneous coronary intervention (PCI) has significantly improved patient outcomes. However, successful re-opening of narrow or blocked coronary arteries does not always restore blood flow to the entire heart muscle.

Our client is developing a first-in-class medical device that will diagnose MVO in real-time during PCI and serve as a treatment platform in the cath lab.

As they roll out their clinical trial across Europe, we are hiring a Senior Clinical Research Specialist to drive clinical activities for this novel technology, oversee and manage clinical trials, and take on advanced proctoring responsibilities.

Responsibilities:

* Train study staff on the correct use of the study device.
* Supervise setup of site workflows to ensure quality data collection.
* Maintain detailed records and documentation.
* Support during live cases to ensure proper use of the device.
* Authorize sites for independent device use in agreement with CPM.
* Join clinical cases to support device use.
* Manage clinical trial activities from initiation to close-out.
* Train and educate staff on study protocols, software, and regulatory requirements.
* Conduct site visits to ensure adherence and data integrity.
* Collaborate with investigators, site staff, and CROs.

Regulatory Requirements Support:

* Assist in IRB submissions and audits.
* Ensure compliance with regulatory standards.

Data Management:

* Ensure accurate data collection and resolve discrepancies.

Qualifications:

* Bachelor’s degree in a relevant field; master’s preferred.
* Experience as Clinical Research Associate, Clinical Specialist, or similar.
* Knowledge of GCP, ISO14155, ICH guidelines.
* Experience in proctoring and site management preferred.
* Strong organizational and communication skills.
* Proficiency with CTMS and EDC software.
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