Catholic Health System
Research Coordinator TRI
Catholic Health System, Buffalo, New York, United States, 14266
Salary: 40,930.50-61,405.50 USD
Facility: Seton Professional Building
Shift: Shift 1
Status: Full Time FTE: 1.000000
Bargaining Unit: Trinity Medical
Exempt from Overtime: Exempt: Yes
Work Schedule: Days
Hours: 8am-4pm, M-F
Summary:
The Research Coordinator is a healthcare position that will involve the participation and coordination of clinical research trials. Work will take place in both a hospital and medical office environment. The key work responsibilities related to this position are primarily intellectual and professional in nature. Successful performance as a Research Coordinator requires the advance knowledge and training in clinical research principles and regulatory compliance requirements. Research Coordinators must be able to work as part of a team as well as autonomously and will be required to frequently exercise discretion and independent judgment.
Responsibilities:
EDUCATION
High school diploma or equivalent
An Associate's degree is required; three (3) to five (5) years of specialized experience and/or training as a Clinical Research Coordinator may be substituted for the advanced education requirement above at the discretion of the Director of Clinical Research
EXPERIENCE
A minimum of two (2) to three (3) years of experience working in a Medical Office environment or Critical Care environment specializing in internal medicine or cardiology is required
Previous training/experience in clinical research is also strongly preferred
Candidates may be credentialed as a Registered Professional Nurse (RN), Certified Research Coordinator (CRC), or Certified Medical Assistant
Candidates should also possess a valid NYS Driver's License
KNOWLEDGE, SKILL AND ABILITY
Knowledge of FDA rules and regulations, GCP, and IRB processes and procedures
Strong interpersonal and organizational skills
Strong written and oral communication skills
Strong computer skills (including MS-Office standard software package)
Able to work well in stressful situations and conditions of frequent interruption.
Regular attendance is an essential function of this position.
Must be willing to travel to multiple office and/or hospital locations to accomplish research, clinical and administrative initiatives
REQNUMBER: 33084
Facility: Seton Professional Building
Shift: Shift 1
Status: Full Time FTE: 1.000000
Bargaining Unit: Trinity Medical
Exempt from Overtime: Exempt: Yes
Work Schedule: Days
Hours: 8am-4pm, M-F
Summary:
The Research Coordinator is a healthcare position that will involve the participation and coordination of clinical research trials. Work will take place in both a hospital and medical office environment. The key work responsibilities related to this position are primarily intellectual and professional in nature. Successful performance as a Research Coordinator requires the advance knowledge and training in clinical research principles and regulatory compliance requirements. Research Coordinators must be able to work as part of a team as well as autonomously and will be required to frequently exercise discretion and independent judgment.
Responsibilities:
EDUCATION
High school diploma or equivalent
An Associate's degree is required; three (3) to five (5) years of specialized experience and/or training as a Clinical Research Coordinator may be substituted for the advanced education requirement above at the discretion of the Director of Clinical Research
EXPERIENCE
A minimum of two (2) to three (3) years of experience working in a Medical Office environment or Critical Care environment specializing in internal medicine or cardiology is required
Previous training/experience in clinical research is also strongly preferred
Candidates may be credentialed as a Registered Professional Nurse (RN), Certified Research Coordinator (CRC), or Certified Medical Assistant
Candidates should also possess a valid NYS Driver's License
KNOWLEDGE, SKILL AND ABILITY
Knowledge of FDA rules and regulations, GCP, and IRB processes and procedures
Strong interpersonal and organizational skills
Strong written and oral communication skills
Strong computer skills (including MS-Office standard software package)
Able to work well in stressful situations and conditions of frequent interruption.
Regular attendance is an essential function of this position.
Must be willing to travel to multiple office and/or hospital locations to accomplish research, clinical and administrative initiatives
REQNUMBER: 33084