Clinical Trial Coordinator
PPD is proud to employ over 20,000 employees worldwide,
across 47 countries and 89 offices. In just over 30 years, PPD has grown to become a leading U.S.
based CRO and recently has won accolades for industry leading CRA team, employee training &
development, excellence in service and numerous awards for Best CRO. Our sustained year on year
growth means that we are always looking for exceptional clinical talent to join our
company.
Since opening in 2007, PPD’s offices in China now
include 20 different departments. The combined Beijing and Shanghai offices are now seven times
the size they were two years ago and are continuing to grow. In 2018 alone, the Clinical
Management team is expected to triple in size. PPD China is able to offer our staff opportunities
to collaborate on projects not only in Asia Pacific, but in regions around the world. You’ll have
the opportunity to work on multinational trials—with top-tier sponsors, and on an
industry-leading platform.
This is a great time to join PPD China. Currently PPD
is recruiting for Project Assistant to join our Clinical Monitoring department. From our office
in Beijing to Shanghai, this department defines and develops clinical programs in China. We
ensure the highest-quality review of data and effective interaction with study sites, including
on-site monitoring throughout a study. Our clinical research associates (CRAs), remote site
monitors (RSMs), project assistants (PAs), and client-dedicated teams oversee and administer the
health and efficacy of treatments during trials. We support the logistics and organization of
clinical sites—ensuring that patients receive needed care, as well as identifying and treating
clinical trial participants
Essential Functions and Other Job
Information:
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Coordinates, oversees and completes administrative functions on assigned trials including, but not limited to, reviewing and transmitting regulatory documents, processing documents sent to file, QC and reconciling project reports, performing mass mailings and faxes, managing and distributing paper study supplies to sites.
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Performs PPD Investigator file reviews and logs findings in CTMS.
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Maintains assigned data points within CTMS according to the established conventions within specified times.
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Coordinates team conference calls, documents, completes and distributes meeting minutes from internal/client meetings.
Education and Experience:
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Bachelor’s Degree preferred or good general education, combined with evidenced administrative competence and relevant IT skills. In all cases, the combination of education, training and experience provides the individual with the required knowledge, skills and abilities to do the job. General administrative experience preferrably in clinical research administration.
Knowledge, Skills and Abilities:
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Self-motivated, positive attitude with effective oral and written communication and interpersonal skills
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Ability to work in a team or independently, as required
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Good organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively
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Demonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency
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Strong customer focus
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Flexibility to reprioritize workload to meet changing project timelines
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Demonstrated ability to attain and maintain a good working knowledge of applicable FDA
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Regulations, ICH Good Clinical Practices, and PPD/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout.
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Strong English language and grammar skills
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Strong computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems
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Ability to successfully complete PPD clinical training program
Our offer: As a
compensation, you will be provided with a competitive remuneration, corporate trainings and the
opportunity to become a part of a fast growing, multinational company. At PPD, we encourage
our employees to demonstrate creativity, innovation and fresh insights as well as a
solution-focused approach. We also value teamwork, camaraderie and enthusiasm. This is
a full-time, permanent position.
Locations we are hiring in are:
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Office based Beijing
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