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Sr. Clinical Research Coordinator TRI

Location: Buffalo, NY, United States

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Job Description

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:

8:00am to 4:00pm

Summary:

The Senior Clinical 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 Senior Clinical Research Coordinator requires the advance knowledge and training in Cardiology as well as the use of effective clinical research principles and regulatory compliance requirements. The Senior Clinical Research Coordinator 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 preferred; five (5) or more years of specialized experience and/or training as a Clinical Research Coordinator may be considered in lieu of degree

EXPERIENCE
  • A minimum of two (2) years of experience working in a Medical Office environment or Critical Care environment specializing in internal medicine or cardiology
  • Five (5) or more years of experience in clinical research
  • Registered Professional Nurse (RN), Certified Research Coordinator (CRC), or Certified Medical Assistant Credentials preferred
  • Previous experience as the primary research coordinator in IND or IDE protocol
  • Valid NYS Driver's License

KNOWLEDGE, SKILL AND ABILITY
  • Knowledge of FDA rules and regulations, GCP, and IRB processes and procedures
  • Formal CITI training and/or GCP training
  • Training certification in EDC, and IATA. OSHA training current
  • 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
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