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Project Manager
Covance
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Shanghai,
CHN
Clinical Research
The Project Manager is responsible for acting as the secondary liaison between Covance Central Laboratory and Sponsors, to ensure the successful management of global projects through compliance with the CCLS global project management strategy, in order to deliver outstanding customer satisfaction.
Essential Functions
1. Act as secondary liaison between assigned Sponsor(s) and Covance.
2. Accou ... Read More
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Logistic Administrator
Covance
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Shanghai,
CHN
Other
"For Recruiter Use Only" Job Description
Education/Qualifications - Good level of general education (degree) and computer literate in Microsoft office required.
Experience - Prior experience within a transport and logistics related company
- Good knowledge of shipping requirements in China.
Shanghai, CHN
Shanghai, China ... Read More
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Clinical Research Associate I
Covance
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Shanghai,
CHN
Clinical Research
Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, with or without guidance; liaise with vendors; and other duties, as assigned
- Responsible for aspects of registry management as prescribed in the project plans
- General On-Site Monitoring Responsibilities:
o ... Read More
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Clinical Research Associate II
Covance
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Shanghai,
CHN
Clinical Research
- Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned
- Responsible for all aspects of site management as prescribed in the project plans
- General On-Site Monitoring Responsibilities
o Ensure the study staff w ... Read More
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Senior Clinical Research Associate
Covance
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Beijing,
CHN
Clinical Research
Job Summary:
- Assures the implementation of project plans as assigned.
- Function as leader for projects of limited scope as assigned.
- Assume line management responsibilities as assigned.
- Site administration and site monitoring responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP.
- Site management responsibility for clinical stu ... Read More
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Clinical Data Coordinator II
Covance
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Beijing,
CHN
Clinical Research
At Covance, your imagination, your dedication, and your drive to find solutions to challenging projects begin on your very first day. Covance is one of the world's largest and most respected contract research organizations. Our clients are a Who's Who of the pharmaceutical and biotechnology industry. If you're looking for a diverse and stimulating work environment, you'll find it at Covance.
Exci ... Read More
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Statistical Programmer I
Covance
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Beijing,
CHN
Clinical Research
I. Job Summary:
The role of the post holder is to assist in the provision of a Statistical Programming service. The primary activity of the Statistical Programmer is to develop and review SAS® programs and output for the management and reporting of clinical trial data.
A. Duties and Responsibilities:
- Ensure quality of personal work.
- Interact with project team members in related discipline ... Read More
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Clinical Data Coordinator
Covance
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Beijing,
CHN
Clinical Research
- Review clinical trial data in accordance with [Global] Data Management Plans and applicable standardized data management processes (SOPs, Work Instructions, etc.) to identify erroneous, missing, incomplete, or implausible data
- Run ancillary programs (e.g., diagnostics, special listings, reconciliation discrepancy listings) used to support the review of clinical trial data
- Generate, resol ... Read More
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Technologist 1
Covance
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Shanghai,
CHN
Medical Technologist
Job Description
POSITION MAIN OBJECTIVES
Ensure performance of laboratory testing according to quality standards in place as well as to quality assurance/control procedures
MAIN RESPONSIBILITIES
Perform laboratory testing
Ensure the validity and the reliability of results
Optimize reagents management
Maintain equipments and instruments
Document work as needed
Comply with safety rules
MAIN TA ... Read More
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Clinical Data Coordinator II
Covance
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Beijing,
CHN
Clinical Research
- Review clinical trial data in accordance with [Global] Data Management Plans and applicable standardized data management processes (SOPs, Work Instructions, etc.) to identify erroneous, missing, incomplete, or implausible data
- Run ancillary programs (e.g., diagnostics, special listings, reconciliation discrepancy listings) used to support the review of clinical trial data
- Generate, resol ... Read More
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