Research Coordinator 1-Pediatrics - Infectious Disease
Memphis, Tennessee
Employer: University of Tennessee
Industry:
Salary: $21.69 per hour
Job type: Full-Time
Market Range: 08
Hiring Salary: $21.69/Hourly
THIS IS A GRANT FUNDED POSITION
JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: The Research Coordinator 1 recruits young children with a first acute respiratory virus infection (RSV, SARS-CoV-2, influenza) in the Emergency Department and inpatient floors at Le Bonheur. This position approaches prospective subjects, discuss study with parents/guardians, and obtains informed consent. This position creates and maintains a database for the storage of patient information as enter and check data in the database.
DUTIES AND RESPONSIBILITIES:
Qualifications:
MINIMUM REQUIREMENTS:
EDUCATION: Bachelor's Degree. (TRANSCRIPT REQUIRED)
EXPERIENCE: One (1) year of research experience in subject recruitment, informed consent, understanding of IRB requirements, and following a research study protocol; OR a combination of education, training, and experience to equal five (5) years.
KNOWLEDGE, SKILLS, AND ABILITIES:
• Knowledge of study protocol to supervise, perform, and carry out study procedures.
• Ability to obtain informed consent and document the process according to policies of the UT IRB and Methodist Le Bonheur Hospital.
• Knowledge of IRB and other regulatory requirements.
• Ability to establish and maintain good relationships in multidisciplinary team.
• Ability to maintain contact with enrolled families to facilitate follow-up.
• Acquire skill in creating/editing online case report forms in REDCap (with training) and enter and maintain data integrity.
• General computer skills including Microsoft Office especially Word and Excel.
Hiring Salary: $21.69/Hourly
THIS IS A GRANT FUNDED POSITION
JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: The Research Coordinator 1 recruits young children with a first acute respiratory virus infection (RSV, SARS-CoV-2, influenza) in the Emergency Department and inpatient floors at Le Bonheur. This position approaches prospective subjects, discuss study with parents/guardians, and obtains informed consent. This position creates and maintains a database for the storage of patient information as enter and check data in the database.
DUTIES AND RESPONSIBILITIES:
- Plans and monitors the recruitment timetable in collaboration with the PI; submits weekly recruitment numbers/results to the PI.
- Reviews consents and data collected for study subjects for each study visit.
- Creates and maintains study logs for effective trial management; troubleshoots patient management problems/scheduling conflicts, etc. for assigned project(s).
- Devises and implements protocols and data gathering methods.
- Conducts protocol specific patient visits.
- Reviews and maintains source documentation and case report forms for completion and ensures confidentiality of subject records.
- Oversees the study lab specimens are collected/sent in an appropriate manner.
- Collects nasal swabs from study subjects.
- Submits orders for supplies of assigned projects.
- Complies with the Clinical Trials Unit Manual of Procedures (MOP).
- Communicates with St. Jude study coordinators and research manager regarding IRB related issues.
- Gathers information for chart reviews, site visits, etc. as needed and distributes requested information appropriately.
- Performs yearly follow-up study visits and procedures as required by the study protocol.
- Performs other duties as assigned.
Qualifications:
MINIMUM REQUIREMENTS:
EDUCATION: Bachelor's Degree. (TRANSCRIPT REQUIRED)
EXPERIENCE: One (1) year of research experience in subject recruitment, informed consent, understanding of IRB requirements, and following a research study protocol; OR a combination of education, training, and experience to equal five (5) years.
KNOWLEDGE, SKILLS, AND ABILITIES:
• Knowledge of study protocol to supervise, perform, and carry out study procedures.
• Ability to obtain informed consent and document the process according to policies of the UT IRB and Methodist Le Bonheur Hospital.
• Knowledge of IRB and other regulatory requirements.
• Ability to establish and maintain good relationships in multidisciplinary team.
• Ability to maintain contact with enrolled families to facilitate follow-up.
• Acquire skill in creating/editing online case report forms in REDCap (with training) and enter and maintain data integrity.
• General computer skills including Microsoft Office especially Word and Excel.
Created: 2024-09-18
Reference: 24000001WP
Country: United States
State: Tennessee
City: Memphis
ZIP: 38120
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