CRA II

🕒 June 1

🇨🇳 China – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 45%

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Conduct 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 monitoring tools, procedures, and processes, including monitoring plans, checklists, and templates • Contribute to the design, implementation, and delivery of processes, programs, and policies • Participate in developing standard operating procedures (SOPs) and training materials • Manage defined components of projects or processes, including coordinating site visits, tracking study progress, and resolving issues • Ensure accurate and timely documentation of monitoring activities and findings • Write monitoring reports, follow-up letters, and action plans • Collaborate with cross-functional teams, investigators, site staff, and other stakeholders to support clinical trial operations

🎯 Requirements

• 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 • Certified Clinical Research Associate (CCRA) or equivalent certification preferred • 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

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition and total rewards program • Inclusive culture • Reasonable accommodations, when appropriate, for employees or applicants with disabilities

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