Tulane University
Clinical Protocol Technician – Tulane University
2 days ago – among the first 25 applicants
Summary The Clinical Protocol Technician for Trauma Research in the Department of Surgery will assist investigators with enrolling patients in emergency clinical trials. The technician will screen and enroll patients arriving at the Trauma Center under Exception from Informed Consent (EFIC). Additional responsibilities include data collection and entry, processing of blood samples, administering pre or post‑enrollment informed consent to subjects and/or legally authorized representatives, and informing patients or their representatives of the patient’s enrollment into an emergency clinical trial via EFIC.
This position is for the night shift Monday–Friday, with rotating weekends, 11:00 pm to 7:30 am.
Required Knowledge, Skills, and Abilities
Ability to work in a fast‑paced environment and patient‑centered atmosphere.
Solid analytical skills and attention to detail.
Excellent oral and written communication skills.
Proficient computer keyboarding skills; working knowledge of Microsoft Word, Excel, PowerPoint, and Access.
Familiarity with standard electronic office machines (phones, copiers, fax).
Required Education and/or Experience
High School Diploma or equivalent with prior clinical work experience.
OR current undergraduate student in a biological science related field.
OR Bachelor’s Degree.
Preferred Qualifications
Expressed interest in Clinical Research.
Motivated to learn about Clinical Research and associated regulations.
Bachelor’s degree in a biological science related field.
Seniority level Entry level
Employment type Full‑time
Job function Health Care Provider
Industries Higher Education
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Summary The Clinical Protocol Technician for Trauma Research in the Department of Surgery will assist investigators with enrolling patients in emergency clinical trials. The technician will screen and enroll patients arriving at the Trauma Center under Exception from Informed Consent (EFIC). Additional responsibilities include data collection and entry, processing of blood samples, administering pre or post‑enrollment informed consent to subjects and/or legally authorized representatives, and informing patients or their representatives of the patient’s enrollment into an emergency clinical trial via EFIC.
This position is for the night shift Monday–Friday, with rotating weekends, 11:00 pm to 7:30 am.
Required Knowledge, Skills, and Abilities
Ability to work in a fast‑paced environment and patient‑centered atmosphere.
Solid analytical skills and attention to detail.
Excellent oral and written communication skills.
Proficient computer keyboarding skills; working knowledge of Microsoft Word, Excel, PowerPoint, and Access.
Familiarity with standard electronic office machines (phones, copiers, fax).
Required Education and/or Experience
High School Diploma or equivalent with prior clinical work experience.
OR current undergraduate student in a biological science related field.
OR Bachelor’s Degree.
Preferred Qualifications
Expressed interest in Clinical Research.
Motivated to learn about Clinical Research and associated regulations.
Bachelor’s degree in a biological science related field.
Seniority level Entry level
Employment type Full‑time
Job function Health Care Provider
Industries Higher Education
#J-18808-Ljbffr