Research Assistant - 253263

Benefits

Qualifications

• •Demonstrates proficiency at performing basic clinical procedures such as vital signs, ECGs, and sample processing

Responsibilities

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