Job Title: Clinical Research Associate Job Location: China Job Overview: The CRA monitors investigational sites to ensure subject safety and provide quality data review and reporting in compliance with the Caidya and/or client Standard Operating Procedures (SOPs),
Job Overview: Lead RFP/RFI development processes and timelines to support an efficient, high quality and timely proposal submission and scope change process. Lead initiatives to maximize the quality of the proposal submission. Train/mentor other proposal analyst
Job Overview: The Project Manager (PM) fulfills the requirements of managing clinical trials (typically at the country or regional level) to ensure timely delivery of project required objectives and timelines within the scope of the client
Job Overview: Lead RFP/RFI development processes and timelines to support an efficient, high quality and timely proposal submission and scope change process. Lead initiatives to maximize the quality of the proposal submission. Train/mentor other proposal analyst
Job Title: Statistical Programmer II Job Location: Chengdu，China Job Overview: The Statistical Programmer II is responsible for programming activities for the data preparation and analysis of clinical data. Duties include creation and validation of datasets, tables,
Job Title: Senior Clinical Research Physician (SCRP) Job Location: China, homebased Job Overview: The SCRP is a Medically Qualified person without or with limited experience in a drug development/drug safety environment or medical data review. SCRP
Job Overview: The Position will oversee the cross-functional execution of Clinical Contracts to ensure consistency and quality while identifying and solving any issues that potentially would delay the negotiation and execution of site contracts. CM acts
Job Overview: The Senior Clinical Research Associate monitors investigational sites to ensure subject safety and provide high quality data review and reporting in compliance with the Company and/or client Standard Operating Procedures (SOPs), Good Clinical Practice
Planning/Controlling (Scheduling and Resource Management) •Responsible for coordinating, monitoring and reporting project schedule and resource management information to enable alignment of PRD and partner line schedules and FTE/dollar resources. These schedules include: •Clinical study plans (Protocol
Job Description • Translates team’s strategic objectives into operational plans; • provides insight into operational feasibility of proposed strategies. • Drives cross-functional and cross-geographical alignment to strategic plans and goals. • Recognizes and flags internal or
Job Overview: The Contracts Manager (CM) will oversee the cross-functional execution of Clinical Contracts to ensure consistency and quality while identifying and solving any issues that potentially would delay the negotiation and execution of site contracts.
Job Overview: A Director of Regulatory and Strategic Development will be responsible for the primary delivery of or oversight and management of allocated projects including regulatory authority licenses, registrations, exemptions, designations, applications or authorizations for marketing