Role Overview:
MakroCare is seeking a highly skilled Senior Clinical Research Associate (CRA) to join our team as a consultant in Shanghai China. The CRA will manage daytoday clinical trial activities ensuring compliance with protocols and regulatory requirements. This role involves protocol review trial design and implementation collaboration with clinical operations teams conducting research and providing scientific support.
Key Responsibilities:
Manage daily clinical trial operations and ensure compliance with study protocols.
Review clinical trial protocols and participate in the design and of clinical studies.
Collaborate with clinical operations teams providing support throughout the trial lifecycle.
Conduct site monitoring as required following instructions from the Project Manager (likely once or twice monthly).
Perform data analysis interpret results and contribute to research efforts.
Liaise with the medical and scientific community to provide necessary trial support.
Qualifications:
Bachelor s or Master s degree in a related scientific field.
410 years of experience as a Clinical Research Associate.
Strong knowledge and handson 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.
Ability to work independently and remotely.
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