We’re a global, mid-size CRO that pushes boundaries, innovates, and invents - because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe, but by those who take pioneering, creative approaches, and implement them with quality and excellence. We are experts, bright thinkers, dreamers, and doers. Together, we are changing the way the world experiences CROs, in the best possible way.

*This virtual position is home-based!

Note: We are accepting resumes (CV) from experienced CRAs in Southeast US

Worldwide Clinical Trials is powered by proactive insight - the scientific and therapeutic expertise to challenge assumptions, to ask the right questions, to find the answers. It is driven by rigorous operations on a global scale to ensure quality data and predictable, cost-efficient outcomes. And it is championed by a team that is “all in” and never satisfied. We know every trial can introduce unexpected challenges, but we tackle those confidently with the tenacity, creativity, flexibility, and agility that set Worldwide apart.

Our Clinical Research Associates (CRA) will ideally have 2+ years of experience in field monitoring for site qualification, initiation, interim monitoring, site management and study close-out visits for studies in accordance with Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs). Our CRAs are responsible for the quality of data submitted from study sites. In addition, CRAs must assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.2+ years of experience as a Clinical Research Associate

Our CRAs are home-based. Experience in CNS is preferred.

Requirements:

• 2+ years of experience as a Clinical Research Associate
• 4-year university degree
• Experience in Alzheimer's Disease preferred
• Willingness to travel required
  We’re a global, mid-size CRO that pushes boundaries, innovates, and invents - because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe, but by those who take pioneering, creative approaches, and implement them with quality and excellence. We are experts, bright thinkers, dreamers, and doers. Together, we are changing the way the world experiences CROs, in the best possible way.
  
  *This virtual position is home-based!
  
  Note: We are accepting resumes (CV) from experienced CRAs in East Coast US
  
  Worldwide Clinical Trials is powered by proactive insight - the scientific and therapeutic expertise to challenge assumptions, to ask the right questions, to find the answers. It is driven by rigorous operations on a global scale to ensure quality data and predictable, cost-efficient outcomes. And it is championed by a team that is “all in” and never satisfied. We know every trial can introduce unexpected challenges, but we tackle those confidently with the tenacity, creativity, flexibility, and agility that set Worldwide apart.
  
  Our Clinical Research Associates (CRA) will ideally have 2+ years of experience in field monitoring for site qualification, initiation, interim monitoring, site management and study close-out visits for studies in accordance with Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs). Our CRAs are responsible for the quality of data submitted from study sites. In addition, CRAs must assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.2+ years of experience as a Clinical Research Associate
  
  Our CRAs are home-based. Experience in Psychiatry/Depression is preferred.
  
  Requirements:
  
  • 2+ years of experience as a Clinical Research Associate
  • 4-year university degree
  • Strong CNS Experience preferred
  • Willingness to travel required
  
  
  

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