The EMT/Paramedic will have various clinical study activities to support the conduct of clinical studies. This role involves providing comprehensive Quality Control (QC) activities related to the completion of source documents and Case Report Forms (CRFs) for clinical trials.
ResponsibilitiesAssist the Clinical Research Coordinator (CRC) and Investigator with clinical study activities.Provide comprehensive Quality Control (QC) activities for the completion of source documents and CRFs.Conduct phlebotomy and blood draws as needed.Ensure compliance with clinical research Good Clinical Practice (GCP) requirements and medical documentation standards.Essential SkillsIntermediate to advanced knowledge of Internet technology.Strong interpersonal skills.Detail-oriented with strong document review skills.Training or experience in clinical research GCP requirements and medical documentation.Experience with IV procedures.Phlebotomy and blood draw skills.Additional Skills & QualificationsWillingness to obtain Basic Life Support (BLS) and Advanced Cardiovascular Life Support (ACLS) certifications before becoming permanent.Customer service experience.Work Environment
This is a full-time overnight position (approximately 36 hours per week), with shifts on Friday, Saturday, and Sunday from 7:00 PM to 7:00 AM, including a 30-minute unpaid meal break. The candidate must be able to train during their first three weeks on the day shift, Monday to Friday, from 8:00 AM to 4:30 PM, with a 30-minute lunch break. The work environment is a 24-hour clinical research facility with a clinic-type setting and a total of 80 employees on-site. The dress code is business casual, with no jeans allowed.
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