Job Description
Our Clinical Research Assistant is a specialized research professional working with and under the direction of the Principal Investigator (PI), Clinical Research Manager, and Clinical Research Coordinators (CRCs). The Clinical Research Assistant is responsible for supporting the assessment, planning, implementation, and execution of research protocols.
Schedule: Monday through Friday (on-site)
What You'll Do:
- Assists CRCs, Principal Investigator (PI), and Sub-Investigators with initiation and maintenance of study protocols
- Assists with procedures throughout study visits including, but not limited to, collection of vitals and ECGs, phlebotomy, blood processing, collection of height and weight, conducting subject questionnaires, and other protocol specific items.
- Assists CRCs with completing study source documentation, data entry into electronic data capture (EDC) systems, and maintenance of study files.
- Assists with study visits per study protocol, inclusive of source document and case report form completion and submission
- Process blood, urine, and biopsy samples in accordance with study protocols and IATA/OSHA standards.
- Assists with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol.
Skills and Experience:
- Bachelor’s degree or equivalent preferred
- Minimum of 1 year of directly related experience required
- Bilingual in Spanish preferred
In support of our mission statement, "Healthier Practices, Healthier Patients," we have a Tobacco Free Environment. We prefer NOT to hire tobacco and nicotine users, includes vaping/e-cigarettes.
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