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Clinical Research Associate
1 month ago
At Worldwide Clinical Trials, we're a global team of over 3,500 experts who are passionate about changing the way the world experiences CROs. We're a company that values quality, excellence, and pioneering approaches to clinical research.
Our MissionWe believe that everyone plays a crucial role in making a world of difference for patients and their caregivers. Our mission is to advance clinical research and make a meaningful impact on people's lives.Job Summary
We're seeking a highly skilled Clinical Research Associate to join our team. As a CRA, you'll work alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. You'll be responsible for conducting site qualifications, initiation, interim monitoring, site management, and study close-out visits.
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.
- Compile and ensure completeness of regulatory documents and ethical submission documentation.
- Excellent interpersonal, oral, and written communication skills in English and local language.
- Broad understanding of clinical research principles and process.
- Proficiency in Microsoft Office, CTMS, and EDC Systems.
We offer an unparalleled experience where you can drive remarkable scientific breakthroughs and be at the core of every successful clinical trial. You'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment.