50% Clinical/HC Research Associate - Cardiology
About The Position
BASIC FUNCTION: Apply clinical skills requiring specialized licensing to deliver and evaluate research protocols. The position requires the academic knowledge of a specific discipline and professional licensure in a clinically-related field related to the study. Key areas of responsibility include research/clinical activities, protocol development and study responsibilities, subject recruitment and enrollment, data collection and monitoring, regulatory guidelines and documents, human resources/leadership and financial responsibility. KEY AREAS OF RESPONSIBILITY: Research/Clinical Activities: Perform clinical and translational research studies. Protocol Development and Study Responsibilities: Assist in protocol development and provide input into descriptions of routine research procedures. Subject Recruitment and Enrollment: Schedule trial related procedures and visits. Data Collection and Monitoring: Collect and enter clinical and translational research data required by the sponsors in a timely manner. Regulatory Guidelines and Documents: Report any reportable events to appropriate parties. Human Resources/Leadership: Provide direction, assignments, feedback, coaching and counseling to assure outcomes are achieved. Financial Responsibility: Contribute to identification of increased cost/inefficient spending and cost containment measures.
Requirements
- A Bachelor's degree or an equivalent combination of education and experience.
- Excellent written and verbal communication skills are required.
- Certification by the American Registry of Diagnostic Medical Sonographers or other nationally recognized accreditation organizations for primary specialty.
- At least two year’s experience acquiring and analyzing cardiac ultrasound images.
- Excellent written and verbal communication skills are required.
Nice To Haves
- Registered Diagnostic Cardiac Sonographer certification.
- Registered Vascular Technologist certification.
Responsibilities
- Perform clinical and translational research studies.
- Assist in protocol development and provide input into descriptions of routine research procedures.
- Schedule trial related procedures and visits.
- Collect and enter clinical and translational research data required by the sponsors in a timely manner.
- Report any reportable events to appropriate parties.
- Provide direction, assignments, feedback, coaching and counseling to assure outcomes are achieved.
- Contribute to identification of increased cost/inefficient spending and cost containment measures.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
5,001-10,000 employees
