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SAS Programmer

Responsibilities:

1 Build standard tabulation datasets according to specific industry standards or the format requested by clients.
2 Develop SAS programs to produce data listings and case report form tabulations.
3 Develop SAS programs to implement statistical analysis as specified in the statistical analysis plan and table shells.
4 Build analysis datasets according to specific industry standards or the format requested by clients.
5 Review the standard tabulation datasets and/or analysis dataset development plan and SAS programs created by other SAS programmers.
6 Perform the validation and quality assurance aspects of all SAS programming activities.
7 Represent the SAS programming team at project team meetings and provide updates to the project team on task status.
8 Ensure that the SAS programming needs of projects are met, reporting all concerns to the Head of Biostatistics in order to resolve clinical team and/or client issues quickly.
9 Communicate with other project members regarding project issues.
10 Communicate with the client regarding SAS programming issues.
11 Ensure adherence to all timelines associated with SAS programming.
12 Ensure the integrity of all systems by maintaining security and following change control procedures.
13 Perform other duties assigned by the supervisor.

Qualifications:

1 Bachelor's degree in a scientific or technical area (an advanced scientific degree in biostatistics or statistics is desirable).
2 Minimum of 3 years of SAS programming experience as it pertains to clinical trials conducted in the pharmaceutical, biotech, or medical device industry. Previous experience managing SAS programmers is desirable.
3 Excellent ability to plan, manage, and coordinate SAS programming activities in clinical trials.
4 Excellent ability to manage and resolve SAS programming issues.
5 Good at dealing with sensitive inquiries or complaints from clients or potential clients and protecting confidentiality.
6 Must have team-building skills and demonstrate the ability to work successfully in a team environment.
7 Knowledgeable in all aspects of the federal (FDA) regulations and requirements governing the conduct of drug, medical device, and biological studies, including, but not limited to, ICH-GCP guidelines.
8 Must have a good command of the English language.

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