Senior Clinical Research Associate
hace 1 mes
At Worldwide Clinical Trials, we are seeking a highly skilled Senior Clinical Research Associate to join our team. As a key member of our clinical operations team, you will be responsible for ensuring the successful execution of our clinical research programs.
Key Responsibilities:
- Conduct 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
- Broad understanding of clinical research principles and process
- Proficiency in Microsoft Office, CTMS, and EDC systems
Education:
- Four-year college curriculum in life sciences
- Two-year college curriculum or equivalent education/training (nursing degree or equivalent life science degree) and one year experience with clinical research
About Us:
Worldwide Clinical Trials is a leading global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications from discovery to reality.
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