Research Assistant - Santa Clara, CA (95050)
Format: 5 month contract with possibility of extension/conversion
Hours: Monday - Friday, 2 shifts: 6am-2pm, 2pm-10:30pm
Pay: $21/hour
Responsibilities:
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Understands the main objectives of each ongoing study and the study procedures for which he/she will be responsible.
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Demonstrates proficiency at performing basic clinical procedures such as vital signs, ECGs, phlebotomy (not required), and sample processing.
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Demonstrates proficiency in documenting observations and study procedures correctly and legibly in the source document.
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Understands and demonstrates proficiency in appropriately responding to medical emergencies onsite.
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Performs study procedures as assigned.
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Observes and records data related to patient safety and study procedures.
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Ensures that all study data is recorded accurately and completely.
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Assists nursing staff and Clinical Project Managers with study procedures and patient management as directed.
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Assists in the transcription of study data from source documents to Case Report Forms (CRFs)/ (eCRFs).
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Understands and complies with Good Clinical Practices (GCPs), particularly those regarding the protection of human subjects and integrity of clinical trial data.
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Understands and complies with Standard Operating Procedures (SOPs) and Work Instructions (WIs).
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Participates as requested in Continuous Quality Improvement (CQI) process.
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Flexibility to work mornings, evenings, and/or overnight shifts as needed.
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Attends and participates in all required training activities.
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Participates as requested as a Clinical Operations Study Liaison.
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Assists with Screening Receptionist duties and responsibilities as requested.
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Assists with Recruitment duties and responsibilities as requested.
Required Skills:
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Demonstrates proficiency at performing basic clinical procedures such as vital signs, ECGs, and sample processing.
Preferred Skills: