Sr Clinical Research Associate - Direct Hire - US

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Job Responsibilities:

• Conduct qualification visits (QV) site initiation visits (SIV) monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports
  
• Oversee integrity of the study and utilize problemsolving skills to promote rapport with the site and staff
  
• Review the performance of the trial at designated sites ensure the rights and wellbeing of human subjects are safeguarded and are in accordance with the protocol
  
• Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines while also ensuring compliance with the approved SOPs protocol/amendment(s) GCP and the applicable regulatory requirements
  
• Evaluate the quality and integrity of the reported data site efficacy and drug accountability
  
• Monitor completeness and quality of regulatory documentation and perform site document verification
  

Job Qualifications:

• Bachelors degree in scientific discipline
  
• 1.5 yrs experience monitoring in clinical research as a Clinical Research Associate (CRA)
  
• Ability to work in selfdriven capacity with a sense of urgency and limited need for oversight
  
• The ability to manage multiple tasks evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocols
  
• Strong computer skills including but not limited to the knowledge of CTMS EDMS and MS Excel and Word
  
• A client focused approach to work with a flexible attitude with respect to assignments and new learning