Job Description

USA, (Home-based)

Sr. CRA

Bachelor's degree in scientific discipline + 1.5 yrs experience monitoring in clinical research as a CRA

Direct Hire

Negotiable Salary

(sponsorship not available)

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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 problem-solving skills to promote rapport with the site and staff
  
• Review the performance of the trial at designated sites, ensure the rights and well-being 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
  
• Leverage your expertise
  
• Build relationships
  
• Protect patients
  
• Drive productivity
  
• Ensure quality
  
• Execute
  

Job Qualifications:

• Bachelor's degree in scientific discipline
  
• 1.5 yrs experience monitoring in clinical research as a CRA (Clinical Research Associate)
  
• Ability to work in self-driven 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
  

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