Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world. 

With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research. 

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

Discover the Difference

We love knowing that someone is going to have a better life because of the work we do.  Discover the Difference at Worldwide Clinical Trials. Explore additional opportunities on our careers page, visit http://www.worldwide.com/careers, or connect with us on LinkedIn.