Clinical research Associate I – Beijing

Syneos Health is a leading biopharmaceutical solutions organization that helps customers succeed. We use clinical, medical, and commercial knowledge to deliver results in today’s market.

Our clinical development approach puts the customer and patient first.We constantly look for ways to simplify our work, making Syneos Health easier to work with and for.

Whether you work with us through a Functional Service Provider partnership or a full-service arrangement, you’ll collaborate with dedicated problem-solvers, innovating as a team to help our customers reach their goals. We are flexible and focused on speeding up the delivery of therapies, as we are committed to improving lives.

Join our team of 29,000 employees in 110 countries and discover why WORK HERE MATTERS EVERYWHERE.

Why Syneos Health

• we invest in our people through career development, supportive management, training, recognition programs, and rewards.
• We are dedicated to our Total Self culture – a place where you can be yourself. This culture unites us globally, and we prioritize taking care of our people.
• We are always working to build a better company for our employees and customers. Diversity in thoughts, backgrounds, and cultures helps us create an inclusive surroundings where everyone belongs.

Job Responsibilities

• Monitor clinical research studies on-site and remotely to ensure they follow accepted practices. This includes reviewing study plans, consent forms, and data records.
• Create and use tools and procedures to ensure high-quality monitoring, such as monitoring plans, checklists, and templates.
• Help design, implement, and deliver processes, programs, and policies. This includes creating standard procedures (sops) and training materials.
• Manage parts of projects or processes, like scheduling site visits, tracking study progress, and solving problems.
• Keep accurate records of monitoring activities and findings, including writing reports, follow-up letters, and action plans.
• Work with different teams to support clinical trials, collaborating with investigators, site staff, and others to ensure studies run smoothly.