What Clinical Operations does at Worldwide

At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients.  

As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Neuroscience, Oncology, Cardiovascular, Metabolic and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.   

What you will do

• Responsible for site qualification, initiation, interim monitoring, site management, and study close-out visits. 
• Provide mentoring and guidance to less experienced CRAs and site staff when needed. 
• Document site visit findings via written reports. 
• Assess, monitor, and train study site staff on protocol adherence as required. 
• Review study subject safety information and informed consent. 
• Conduct source document verification for compliance, patient safety, and veracity of data. 
• Review CRFs using paper or electronic data capture systems and assist sites with data query resolution. 
• Provide applicable updates for site related documentation for filing in the Trial Master File (TMF). 
• Ensure site compliance with IP receipt, accountability and return or destruction. 
• Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate. 

What you will bring to the role

• Excellent interpersonal, oral, and written communication skills in English
• Superior organizational skills with attention to details
• Ability to work with little or no supervision
• Proficiency in Microsoft Office, CTMS and EDC Systems

Your experience

• 2+ years of experience as a Clinical Research Associate
• 4-year university degree or RN/BSN in Nursing
• Experience in Neurology, Oncology and Hematology is required
• Willingness to travel required
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What Clinical Operations does at Worldwide

At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients.  

As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Neuroscience, Oncology, Cardiovascular, Metabolic and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.   

What you will do

• Responsible for site qualification, initiation, interim monitoring, site management, and study close-out visits. 
• Provide mentoring and guidance to less experienced CRAs and site staff when needed. 
• Document site visit findings via written reports. 
• Assess, monitor, and train study site staff on protocol adherence as required. 
• Review study subject safety information and informed consent. 
• Conduct source document verification for compliance, patient safety, and veracity of data. 
• Review CRFs using paper or electronic data capture systems and assist sites with data query resolution. 
• Provide applicable updates for site related documentation for filing in the Trial Master File (TMF). 
• Ensure site compliance with IP receipt, accountability and return or destruction. 
• Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate. 

What you will bring to the role

• Excellent interpersonal, oral, and written communication skills in English
• Superior organizational skills with attention to details
• Ability to work with little or no supervision
• Proficiency in Microsoft Office, CTMS and EDC Systems

Your experience

• 2+ years of experience as a Clinical Research Associate
• 4-year university degree or RN/BSN in Nursing
• Experience in Neurology, Oncology and Hematology is required
• Willingness to travel required
• 
  
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