Senior Data Analyst
May act as the Project Manager for stand-alone data management project(s) · Act as the Lead Data Analyst for assigned data management project(s) · Coordinate the work of Data Management staff assigned to the project · Train assigned employees on project-related data management procedures and guidelines · May have responsibility for the completion ... more
Type: Full Time/Contract Location: Bangalore, Country: United States Posted: 5/16/2008 5:12:17 AM
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Senior Data Analyst
May act as the Project Manager for stand-alone data management project(s) · Act as the Lead Data Analyst for assigned data management project(s) · Coordinate the work of Data Management staff assigned to the project · Train assigned employees on project-related data management procedures and guidelines · May have responsibility for the completion ... more
Type: Full Time/Contract Location: Mumbai, Country: United States Posted: 5/16/2008 5:12:17 AM
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Senior Data Technician
Enter data from Case Report Forms (CRFs) into the database with a high degree of accuracy and speed · Verify data previously entered into the clinical database by performing second entry and resolving discrepancies · As a primary Data Technician for one or more project(s): ¨ Track the progress of CRF ... more
Type: Full Time/Contract Location: Bangalore, Country: United States Posted: 5/16/2008 5:12:17 AM
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Associate Data Analyst
Perform data review and query generation · Assist in defining edit checks to be programmed for the study/project · Review programmed edit checks · Track study progress and issue periodic status reports · Update the database to correct errors · Code Case Report form (CRF) verbatim terms using PharmaNet or sponsor supplied dictionaries · Process ... more
Type: Full Time/Contract Location: Bangalore, Country: United States Posted: 5/16/2008 5:12:17 AM
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Data Technician
Enter data from Case Report Forms (CRFs) into the database with a high degree of accuracy and speed · Verify data previously entered into the clinical database by performing second entry and resolving discrepancies · May act as primary Data Technician for one or more project(s): ¨ Track the progress of ... more
Type: Full Time/Contract Location: Bangalore, Country: United States Posted: 5/16/2008 5:12:17 AM
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Data Analyst
Perform data review and query generation · Define edit checks to be programmed for the study/project · Review programmed edit checks · Track study progress and issue periodic status reports · Update the database to correct errors · Code Case Report Form (CRF) verbatim terms using PharmaNet or sponsor-supplied dictionaries · Process electronic data received ... more
Type: Full Time/Contract Location: Bangalore, Country: United States Posted: 5/16/2008 5:12:16 AM
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Data Analyst
Perform data review and query generation · Define edit checks to be programmed for the study/project · Review programmed edit checks · Track study progress and issue periodic status reports · Update the database to correct errors · Code Case Report Form (CRF) verbatim terms using PharmaNet or sponsor-supplied dictionaries · Process electronic data received ... more
Type: Full Time/Contract Location: Mumbai, Country: United States Posted: 5/16/2008 5:12:10 AM
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Data Technician
Enter data from Case Report Forms (CRFs) into the database with a high degree of accuracy and speed · Verify data previously entered into the clinical database by performing second entry and resolving discrepancies · May act as primary Data Technician for one or more project(s): ¨ Track the progress of ... more
Type: Full Time/Contract Location: Mumbai, Country: United States Posted: 5/16/2008 5:12:10 AM
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Senior Data Technician
Enter data from Case Report Forms (CRFs) into the database with a high degree of accuracy and speed · Verify data previously entered into the clinical database by performing second entry and resolving discrepancies · As a primary Data Technician for one or more project(s): ¨ Track the progress of CRF ... more
Type: Full Time/Contract Location: Mumbai, Country: United States Posted: 5/16/2008 5:12:04 AM
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Clinical Research Associate I
Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 – 50% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines · Recruit investigators for participation in clinical trials · Negotiate study budgets with investigators · Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites · Review ... more
Type: Full Time/Contract Location: Mumbai, Country: United States Posted: 5/16/2008 5:11:58 AM
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Senior Clinical Research Associate
Assist in managing large scale clinical trial projects or function as project manager for small scale projects, ensuring on-time, on-budget performance · Monitor (pre-study, initiation, routine, and close-out visits) investigator sites for GCP compliance according to PharmaNet SOPs and/or client guidelines · Recruit investigators · Negotiate study budgets with investigators · Obtain, review, and ... more
Type: Full Time/Contract Location: Philippines, Country: United States Posted: 5/13/2008 6:57:32 PM
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Manager, Data Management
Participate in the management of the Data Management group · Supervise the Data Management staff for one or more sponsor projects · Assign or act as the Lead Data Analyst as the primary sponsor contact for data management issues/information for each project · Act as the Project Manager for stand-alone data management project(s) ... more
Type: Full Time/Contract Location: Kennett Square, PA Country: United States Posted: 5/12/2008 2:01:09 PM
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Director, Business Development
Generate annual sales per target objective in support of corporate budget
Develop and maintain assigned client relationships using the highest professional standards
Recruit new corporate clients to generate new business opportunities
Develop and conduct client presentations to attract new business and support overall corporate ... more
Type: Full Time/Contract Location: High Wycombe/Frankfurt, Country: United States Posted: 5/9/2008 1:53:08 PM
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Senior Business Development Associate
Support business development efforts to generate annual sales objectives
Develop proposals based on team meetings and discussions, including production of time and budget estimates
Manage the proposal development process and maintain the time-lines for the proposal team
Maintain the Business Development databases that include ... more
Type: Full Time/Contract Location: High Wycombe, Country: United States Posted: 5/9/2008 1:53:08 PM
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Regulatory Associate II
Review regulatory documentation required for the initiation of clinical trials for appropriateness, completeness, and compliance with regulations · Assist in the compilation of regulatory submissions, e.g. INDs/CTAs and NDAs/MAAs · Coordinate submissions to local health authorities, with oversight from management · Coordinate regulatory submissions and contracts with vendors when local submissions require a ... more
Type: Full Time/Contract Location: Princeton, NJ Country: United States Posted: 5/7/2008 3:56:46 PM
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Senior Clinical Research Associate
Assist in managing large scale clinical trial projects or function as project manager for small scale projects, ensuring on-time, on-budget performance · Monitor (pre-study, initiation, routine, and close-out visits) investigator sites for GCP compliance according to PharmaNet SOPs and/or client guidelines · Recruit investigators · Negotiate study budgets with investigators · Obtain, review, and ... more
Type: Full Time/Contract Location: Bangalore, Country: United States Posted: 5/7/2008 2:38:28 AM
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Senior Analyst, Financial Reporting
Prepare monthly, quarterly and annual analysis of consolidated financial statements, including balance sheet, income statement, cash flow, and capital expenditures
Work with operating units to develop and implement reporting to meet internal management needs
Assist with budgeting process, including standardization of budget formats, implementation of budget data into ... more
Type: Full Time/Contract Location: Princeton, NJ Country: United States Posted: 5/7/2008 2:38:12 AM
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Clinical Research Associate II
Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 – 50% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines • Recruit investigators for participation in clinical trials • Negotiate study budgets with investigators • Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites • Review ... more
Type: Full Time/Contract Location: Czech Republic/Slovakia, Country: United States Posted: 5/5/2008 6:52:48 AM
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Senior Clinical Research Associate
Assist in managing large scale clinical trial projects or function as project manager for small scale projects, ensuring on-time, on-budget performance · Monitor (pre-study, initiation, routine, and close-out visits) investigator sites for GCP compliance according to PharmaNet SOPs and/or client guidelines · Recruit investigators · Negotiate study budgets with investigators · Obtain, review, and ... more
Type: Full Time/Contract Location: Bangalore, Country: United States Posted: 5/2/2008 2:52:22 AM
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Clinical Research Associate II
Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 – 50% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines · Recruit investigators for participation in clinical trials · Negotiate study budgets with investigators · Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites · Review ... more
Type: Full Time/Contract Location: Bangalore, Country: United States Posted: 5/2/2008 2:52:16 AM
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