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Senior Clinical Field Specialist, dartford
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Client:
The Mullings Group
Location:
dartford, United Kingdom
Job Category:
Other
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EU work permit required:
Yes
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Job Views:
6
Posted:
26.06.2025
Expiry Date:
10.08.2025
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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 myocardial microvascular obstruction (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 oversee and manage clinical trials for this innovative technology, including advanced proctoring responsibilities.
Responsibilities:
Proctoring and Case Support Duties
* Train study staff on the correct use of the study device.
* Support site setup to ensure quality data collection.
* Maintain detailed records and documentation.
* Assist during live cases to support safe device use.
* Authorize sites for independent device use in agreement with CPM.
* Join clinical cases to ensure proper device application.
Clinical Trial Support
* Manage clinical trial activities from initiation to close-out.
* Train staff on study procedures, software, and regulatory compliance.
* Conduct site visits to monitor adherence and data quality.
* Collaborate with investigators, site staff, and CROs.
Regulatory Requirements Support
* Assist with IRB submissions and audits.
* Ensure compliance with regulatory standards.
Data Management
* Ensure accurate data collection and resolve discrepancies.
* Work with Data Management team for data integrity.
Qualifications:
* Bachelor’s degree in a relevant health science field; master’s preferred.
* Experience as Clinical Research Associate, Specialist, or similar in medical devices or CROs.
* Knowledge of GCP, ISO14155, ICH guidelines, and regulatory requirements.
* Experience in proctoring and site management preferred.
* Strong organizational and communication skills.
* Proficiency in CTMS and EDC software.
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