- Must be able to interact well with patients and the general public
- Excellent organization, analytical, interpersonal, and communication skills
- Ability to maintain confidentiality in all work performed
- Proficient in various software programs (including database management [e.g. Access], presentation packages [e.g. PowerPoint], spreadsheets [e.g. Excel], and advanced word processing [e.g. Word]).Ability to acquire and maintain all required CITI training certificates
- Ability to acquire and maintain credentialing at all required institutions: Tulane Medical Center, Veterans Administration Hospital/New Orleans, LA and University Medical Center.
- Bachelor's Degree or RN with current state licensure at the time of hire; or LPN with current state licensure at the time of hire and three (3) years of related work experience
- Expressed interest in Clinical Research
- Motivated to learn about Clinical Research and associated regulations
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Tulane University New Orleans, United StatesPrecision Health Study (PHS) is a meal-challenge study, with a focus on the dietary glycemic index of carbohydrates. The study lasts around 10 days, including a 7-day usual diet & lifestyle tracking period and a 3-day meal-challenging period. Partici Clinical Research, Research C ...
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Clinical Research Coordinator I, PHS - New Orleans, United States - Tulane University
Description
This is an entry-level coordinator position for the Precision Health Study (PHS). PHS is a meal-challenge study, with a focus on the dietary glycemic index of carbohydrates.The study lasts around 10 days, including a 7-day usual diet & lifestyle tracking period and a 3-day meal-challenging period.
Participants will be recruited in the New Orleans Metropolitan area, via multiple advertisement medium options, which include, but are not limited to:Local newspapers, television, direct mail, and community outreach.
Training will be provided to develop the necessary skills required of a clinical research coordinator.
The primary responsibility of the Clinical Research Coordinator I is to assist in managing all aspects of conducting clinical trials and other epidemiological studies.
The Clinical Research Coordinator I assists with recruitment, screening, enrolling and following study patients, data collection and entry, ensuring protocol compliance and close patient monitoring, all as part of the required learning process required in this primary position for advancement towards a Clinical Research Coordinator II and Clinical Research Coordinator III position.
The Clinical Research Coordinator I assists with all data and source documentation, adverse event reporting and maintenance of complete regulatory files, also as a part of the learning experience.
The Clinical Research Coordinator I will be trained to perform simple procedures (ECGs, vital signs, etc.), as well as laboratory processing.
Selected candidates must complete and pass a background check and an occupational health screening as a condition of employment. For identified jobs, a drug screening will also be required.
The background investigation, required occupational health screening, and any required drug screening will be conducted after a conditional employment offer has been extended.
