Clinical Research Associate II, Global Clinical Trials
hace 16 horas
We are Worldwide Clinical Trials, a global CRO that pushes boundaries and innovates to advance clinical research. As a Clinical Research Associate II, you will be part of a team of over 3,500 experts dedicated to improving lives.
Clinical Operations at Worldwide
You will work alongside brilliant minds across various therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Our collaborative environment ensures that you receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.
Your Key Responsibilities
- Conduct all types of visits, including site qualifications, initiation, interim monitoring, site management, and study close-out visits
- Review study subject safety information and informed consent, and conduct source document verification for compliance, patient safety, and data veracity
- Participate in study team and investigator meetings, and compile and ensure completeness of regulatory documents and ethical submission documentation
Requirements
- Excellent interpersonal, oral, and written communication skills in English and local language
- Superior organizational skills with attention to detail, and the ability to work independently
- Broad understanding of clinical research principles and process
- Proficiency in Microsoft Office, CTMS, and EDC Systems
At Worldwide Clinical Trials, we prioritize cultivating a diverse and inclusive environment where professionals from all backgrounds and experiences can succeed. Join us in shaping the future of clinical research.
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