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What this posting tells you
Mid-level Clinical Research Associate role at PPD Pharmaceutical Development Vietnam. Role supports remote and on-site clinical monitoring ensuring compliance with protocols, GCP and regulations. Position is full-time, remote in Vietnam with office environmental conditions mentioned. Schedule is standard Monday to Friday office hours.
Accounting, Data, Healthcare admin, Operations, Security
Vietnam
Asia/Ho_Chi_Minh
mid-level · full_time
- Compensation is not listed
Accounting hiring on WFH.team
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Explore the remote job marketCRA (Level II) at PPD Pharmaceutical Development Vietnam Company Limited
Work
Schedule
Standard (Mon-Fri) Environmental Conditions Office Job Description Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. e. ). Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability.
Ensures audit readiness. Develops collaborative relationships with investigational sites. Detailed tasks and
Responsibilities
assigned to role are outlined in the task matrix.
Working remotely at PPD Pharmaceutical Development Vietnam Company Limited
PPD Pharmaceutical Development Vietnam Company Limited is hiring for 2 active remote roles, with remote-friendly openings, application links, and job details refreshed from the public remote job inventory.
Remote hiring signal is inferred from active confirmed-remote job listings.