Clinical Research Associate
6 days ago
Job Summary
MakroTech is seeking a highly skilled Clinical Research Associate to manage day-to-day clinical trial activities in Shanghai, China. The ideal candidate will ensure compliance with protocols and regulatory requirements, and have experience in clinical trials and monitoring.
Key Responsibilities
- Manage daily clinical trial operations and ensure compliance with study protocols.
- Review clinical trial protocols and participate in the design and execution of clinical studies.
- Collaborate with clinical operations teams to provide support throughout the trial lifecycle.
- Conduct site monitoring as required, following instructions from the Project Manager.
- Perform data analysis, interpret results, and contribute to research efforts.
- Liaise with the medical and scientific community to provide necessary trial support.
Requirements
- Bachelor's or Master's degree in a related scientific field.
- Minimum of 2 years of experience as a Clinical Research Associate.
- Strong knowledge and hands-on experience in clinical trials and monitoring.
- Proven ability to create, review, and implement clinical trial protocols.
- Experience in clinical operations, including site management, monitoring, and data management.
- Familiarity with Good Clinical Practice (GCP) and International Council for Harmonization (ICH) guidelines.
- Excellent communication, organizational, and analytical skills.
- Ability to work independently and remotely.
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