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Clinical Research Associate
hace 2 meses
As a Clinical Research Associate - Site Management, you will play a vital role in ensuring the quality and excellence of our clinical research programs. You will be responsible for conducting site qualifications, initiation, interim monitoring, site management, and study close-out visits. Your attention to detail and organizational skills will ensure the accuracy and completeness of regulatory documents and ethical submission documentation.
Key Responsibilities- Conduct site qualifications, initiation, interim monitoring, site management, and study close-out visits
- Review study subject safety information and informed consent
- Compile and ensure completeness of regulatory documents and ethical submission documentation
- Excellent interpersonal, oral, and written communication skills in English and local language
- Superior organizational skills with attention to details
- Broad understanding of clinical research principles and process
- Proficiency in Microsoft Office, CTMS, and EDC Systems
At Worldwide Clinical Trials, we offer a unique opportunity to work with a talented team of professionals who share your passion for clinical research. We prioritize cultivating a diverse and inclusive environment that promotes collaboration and creativity. If you are a motivated and detail-oriented individual who is passionate about clinical research, we encourage you to apply for this exciting opportunity.", "lang_code": "en-US"}
