GM6

If any of these postions interest you pm me and I will send you my email address to send me your resume..I wish you luck and I hope you job one of the best companies in the bayarea.
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1. Current Open Position: Senior Software Engineer (San Francisco)

Job Duties:
Over the years Synarc has built several x-ray reading applications. As the number of projects grows, the need for supporting and maintaining these multiple applications grows. While the maintenance needs alone justify having this position, it is critical to develop a scaleable platform for future x-ray/MR/CT etc. reading applications that can support new services that Synarc can offer.

Acquire a good understanding of Synarc business processes and the existing imaging applications. Provide maintenance and support for the applications already deployed. Develop requirements documents jointly with radiologists. Design, develop and test new scaleable imaging applications that support future projects. Work on identifying solutions and implementing these to support future Synarc services including tele-radiology

Requirements:
BS – EE or CS or an MS or higher degree in a scientific field.

5 or more years of software development application.

Experience building medical imaging applications from end-to-end in an industrial setting.

Fluent with object oriented development and web-based development technologies.

Strong knowledge of one more programming languages including Java, C++ or C.

Familiarity with distributed application architectures and knowledge of XML, SOAP, CORBA

Solid understanding of software development life cycle.

Strong communication skills.

Experience within a clinical trials research organization a plus.

Experience working in multi-disciplinary working environments a plus.

Knowledge of Python programming language and/or DICOM standards a plus.
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2.Current Open Position: Research Associate (San Francisco)

Description:
To assure timely delivery of high quality data analysis for clinical trials.

Responsibilities:
Analyze data according to SOP

Load data into study specific databases

Identify and document unacceptable or questionable scans

Maintain database and reconcile discrepancies

Organize forms, hardcopies and electronic media for data tracking

Prepare and distribute study specific documents including QA manual, training materials and other study specific materials

Maintain study documentation according to SOP’s

Request missing or incomplete information

Prepare and document correspondence with sites and sponsors

Certify technologists for study participation

Provide information needed to process IQC data

Provide information necessary to conduct cross-calibration

Support other Research Associates as needed

Monitor and report measures of project performance to Project Manager(s)

Requirements:
Education:
Bachelor’s Degree in Science or health related field; or three years relevant experience

Experience:
Two years experience in clinical research and/or clinical trials

Specialized Abilities:
Knowledge of dual-energy x-ray absorptiometry and its application to clinical trials

Skills:

Sound knowledge of clinical research and GCP requirements

Prior experience in clinical trial management or monitoring preferred

Strong computer skills including word processing, spreadsheets and databases

Detail and accuracy oriented

Verbal and written command of English

Good organizational, interpersonal and team skills

Able to work in a distributed, matrix organization
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GM6

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GM6

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