Biomedical engineers with cardiac device experience
Location: Saint Paul Minnesota
Description: Creative Solutions Services, LLC is at present looking to employ Biomedical engineers with cardiac device experience right now, this career will be placed in Minnesota. For detail informations about this career opportunity kindly read the description below. our client in Mounds View, MN is looking for a Clinical Research Specialist. This is a consulting position. ! If interested, please apply to this ad or send your resume and contact details with the job # and job title in the subject line to recruiter@css-llc.net Clinical Research Specialist I (less than 5 years of experience) Job#: 13-00533 Job Description: Biomedical engineers with cardiac device experience, cardiology nurses, cardiology MDs preferred AND Biomedical engineers with neuromodulation experience, neurology RNs and MDs preferred. • Review and triaging clinical trial deaths and adverse events (AEs) including serious adverse events (SAEs).
- Conduct Case Management in the Clinical Safety Database. • Interacts with investigational sites and field monitors to obtain additional pertinent information as indicated. • Works with the clinical project team to ensure consistency in the assessment, recording and coding of clinical safety events (e.g., SAEs , adverse events (AEs), and device deficiencies). .
- Works with Regulatory Affairs, Clinical Oper! ations and Field Assurance to ensure timely reporting of AEs, ! SAEs and UADEs including expedited and annual reporting and other documents as needed. • Ensures appropriate distribution and notification of SAEs and UADEs to appropriate personnel, partners, and clinical centers for protocol(s). • Liaison for safety-related questions ( e.g., to study team, field support, monitors, and study sites) • Write Clinical Safety plan for assigned protocol(s). • Assists with preparation of assigned section of safety reports for annual reports, clinical study reports, investigator brochure updates, and other documents as required.
- Collaborates with data management and other departments on the development of case report forms, study specific safety reports, and other study specific forms. • Assists with the writing of safety sections of clinical protocols and may present safety monitoring at investigator meetings. • Performs other duties as assigned.
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If you were eligible to this career, please email ! us your resume, with salary requirements and a resume to Creative Solutions Services, LLC.
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This career starts available on: Sat, 08 Jun 2013 11:49:38 GMT
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