Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs. 95% of EMA Authorized Products. Over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
CRA I
Location
China
Posted
5 days ago
Salary
0
Seniority
Mid Level
No structured requirement data.
Job Description
CRA I
Syneos Health
Role Description The CRA I - Urumqi position involves conducting on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices. - Review study protocols, informed consent forms, and case report forms. - Develop and implement tools, procedures, and processes for quality monitoring, including creating monitoring plans, checklists, and templates. - Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materials. - Manage defined components of projects or processes, such as coordinating site visits, tracking study progress, and resolving issues. - Ensure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow-up letters, and action plans. - Collaborate with cross-functional teams to support clinical trial operations, working with investigators, site staff, and other stakeholders to ensure smooth study conduct. Qualifications - Bachelor's degree in a related field or equivalent experience. - Minimum of 2-4 years of experience in clinical research monitoring. - Strong knowledge of Good Clinical Practice (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. Requirements - 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 a team environment. - Strong organizational and time management skills. - Proficiency in Microsoft Office Suite. Benefits - Passionate about developing our people through career development and progression. - Supportive and engaged line management. - Technical and therapeutic area training. - Peer recognition and total rewards program. - Commitment to building an inclusive culture.
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