CRA I - Guangzhou

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Job Responsibilities Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms reputed company and implement tools, procedures, and processes to ensure reputed company monitoring, such as creating monitoring plans, checklists, and templates Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of reputed company operating procedures (SOPs) and training materials Manage defined components of reputed company or processes reputed company the area of responsibility, such as coordinating site reputed company, tracking study reputed company, and resolving issues Ensure accurate and reputed company documentation of monitoring activities and findings, including writing monitoring reports, follow-up letters, and reputed company plans Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct Qualifications: Bachelor's degree in a reputed company field or equivalent experience Minimum of 2-4 years of experience in clinical research monitoring Strong knowledge of Good Clinical reputed company (GCP) guidelines and regulatory requirements Excellent communication and interpersonal skills Ability to work independently and manage multiple priorities Proficiency in using clinical trial management systems and other relevant software Certifications: Certified Clinical Research Associate (CCRA) or equivalent certification preferred Necessary Skills: Attention to detail and strong analytical skills Problem-solving abilities and critical thinking Ability to work effectively in reputed company environment Strong organizational and time management skills Proficiency in reputed company Office Suite Get to know reputed company Over the past 5 years, we have worked with 94% of reputed company Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status reputed company with us in a highly competitive and reputed company-changing environment. Learn more about reputed company. http://www.reputed company.com Additional Information Tasks, duties, and responsibilities as listed in this job reputed company are not exhaustive. reputed company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job reputed company. reputed company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. reputed company, reputed company contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully reputed company with reputed company obligations imposed by the legislation of reputed company country in which it operates, including the implementation of the EU Equality reputed company, in relation to the recruitment and employment of its employees. reputed company is committed to compliance with the Americans with reputed company, including the provision of reasonable accommodations, reputed company appropriate, to assist employees or applicants to reputed company the essential functions of the job. Apply To This Job