Responsibilities include but are not limited to
Patient-Centered Quality and Safety
* Perform all study responsibilities in compliance with the IRB approved protocol
* Document all findings in subject specific source documents
* Provide ongoing assessment of the study subject/patient to identify Adverse Events
* Ensure proper documentation and reporting of all Adverse Events and Serious Adverse Events
* Perform physical examinations as part of screening evaluation and active study conduct
* Provide medical management of adverse events as appropriate
* Complete all study documentation in accordance with the study specific requirements
* Communicate with Sponsors and auditors as requested
* Possess a working knowledge of GCP/ICH guidelines, Clinic SOPs, QA/QC procedures, and Investigator 1572 Form.
* Review Investigator's Brochure prior to performing any study related activities
* Participate in on-call activities as required to ensure adequate medical coverage
* Monitor safety and well-being of study participants at all times
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*Clinical Trials Nurse Practitioner
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Location:
Poway
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Sector:
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Job type:
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Salary:
Negotiable
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Contact:
Pankaj Khatri
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Contact email:
pkhatri@medicalrecruitmentstrategies.com
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Job ref:
BBBH410940_1673368085
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Published:
about 1 year ago
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Expiry date:
2023-03-26
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Client:
Medical Recruitment Strategies