Part 2. Job Openings Continued..
11-17-2003, 10:09 AM
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Part 2. Job Openings Continued..
3. Current Open Position: Research Assistant (San Francisco)
Job Duties:
Assist in the processing and tracking of radiological image data collected in clinical trials
Load CT and MR data
File and archive of study documents and radiographs
Digitization of radiographs
Return radiographs to clinical sites
Initiate necessary preparation of new clinical sites in assigned studies
Assist in the preparation and reproduction of study materials
Providing clinical site personnel help-line assistance throughout the study
Identify and resolve patient data discrepancies for assigned studies
Qualifications:
High School diploma and Associates degree
Strong familiarity with PC-based computers and standard software packages including word processors, spreadsheets, databases; detail and accuracy oriented; self-motivated and ability to work independently with minimal supervision; excellent communication skills.
Medical experience preferred
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4.Current Open Position: Clinical Data Associate (San Francisco)
Reports to: Manager, Clinical Data Management
Major Activities:
Provide CDM support to Synarc personnel and clinical sites
Prepare and maintain key validation documents according to company standards;
Create and update the DMP as needed;
Manage clinical data, track and report progress to PMs and sponsors and ensure timelines are met;
Develop file/format specifications, program data transfer code, QC and process data transfers;
Define, run and review data validation output and resolve discrepant data;
Collaborate with engineering group for development and testing of CDM software tools
Responsibilities:
Meet regularly with Manager, CDM to discuss and seek resolution to project and department issues
Follow up on assigned action items from regularly scheduled department and/or team meetings
Participate in conference calls, sponsor visits, and audits as needed and/or as dictated by contract
Ensure accuracy in manipulation and scrutiny of clinical data
Communicate work performed to Project Manager to ensure appropriate billing
Authority:
Approval of documents, data transfers, and reports sent to the sponsor for projects managed by CDA.
Requirements:
Education: Bachelor Degree in one of the Life or Social Sciences
Experience: 2-4 years of clinical Data Management or university research experience
Specialized Abilities: Experience with relational databases and ability to manipulate data using SAS or SQL preferred
Skills: Strong verbal and written communication ability
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Job Duties:
Assist in the processing and tracking of radiological image data collected in clinical trials
Load CT and MR data
File and archive of study documents and radiographs
Digitization of radiographs
Return radiographs to clinical sites
Initiate necessary preparation of new clinical sites in assigned studies
Assist in the preparation and reproduction of study materials
Providing clinical site personnel help-line assistance throughout the study
Identify and resolve patient data discrepancies for assigned studies
Qualifications:
High School diploma and Associates degree
Strong familiarity with PC-based computers and standard software packages including word processors, spreadsheets, databases; detail and accuracy oriented; self-motivated and ability to work independently with minimal supervision; excellent communication skills.
Medical experience preferred
------------------------------------------------------------------------------------
4.Current Open Position: Clinical Data Associate (San Francisco)
Reports to: Manager, Clinical Data Management
Major Activities:
Provide CDM support to Synarc personnel and clinical sites
Prepare and maintain key validation documents according to company standards;
Create and update the DMP as needed;
Manage clinical data, track and report progress to PMs and sponsors and ensure timelines are met;
Develop file/format specifications, program data transfer code, QC and process data transfers;
Define, run and review data validation output and resolve discrepant data;
Collaborate with engineering group for development and testing of CDM software tools
Responsibilities:
Meet regularly with Manager, CDM to discuss and seek resolution to project and department issues
Follow up on assigned action items from regularly scheduled department and/or team meetings
Participate in conference calls, sponsor visits, and audits as needed and/or as dictated by contract
Ensure accuracy in manipulation and scrutiny of clinical data
Communicate work performed to Project Manager to ensure appropriate billing
Authority:
Approval of documents, data transfers, and reports sent to the sponsor for projects managed by CDA.
Requirements:
Education: Bachelor Degree in one of the Life or Social Sciences
Experience: 2-4 years of clinical Data Management or university research experience
Specialized Abilities: Experience with relational databases and ability to manipulate data using SAS or SQL preferred
Skills: Strong verbal and written communication ability
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