Job Opportunities
At QDS, our continued growth and success are based on the contribution of each and every employee. Our competitive advantage has always been our tremendous intellectual capital, and focus on the employee is key to our ongoing success.
We are committed to attracting and retaining the best talent by:
- Valuing and rewarding individual and team contributions
- Fostering creativity and risk taking
- Encouraging diversity and equal employment opportunity
- Offering competitive compensation packages
- Supporting balanced work-life initiatives
Apply online by sending your resume with cover letter to info@qdservices.com and please state your area/position of interest.
January 2012 - QDS currently has open positions for:
POSITION: CLINICAL MANAGER
Quality Data Services, Inc. is seeking a Clinical Manager with potential for permanent placement.
RESPONSIBLITIES:
Responsible for management of clinical trial operations including oversight of the in-house and regional clinical study team as well as investigative sites. Enforces adherence to SOPs, GCPs and FDA regulations.
Oversee study timelines, project deliverables and scope of services.
Analyze and evaluates clinical data. Ensures compliance with protocol and overall clinical objectives.
Manage process of identifying, qualifying, initiating, monitoring, and closing out of appropriate investigational sites for clinical trials.
Monitor sites in order to ensure that studies are carried out according to the study protocol, SOPs, applicable regulations and the principles of Good Clinical Practice.
Facilitate initial IRB submissions and ensure continuing review with IRB is maintained.
Responsible for collecting, monitoring, processing, and distributing adverse event reports and information queries for investigational and marketed products.
REQUIREMENTS:
Bachelor Degree in health/life sciences preferred or equivalent theoretical/technical depth.
Minimum of 3 years clinical trial management experience with at least one year in a CRO environment and previous monitoring experience.
Proficiency in clinical research, ability to multi-task and working knowledge of FDA/ICH/GCP guidelines.
Competitive salary.
Local candidates preferred.
Must be able to work unrestricted in the US.
No agencies.
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POSITION: DATA MANAGER
Quality Data Services, Inc. is seeking a contract Data Manager with potential for permanent placement.
RESPONSIBLITIES:
Manages data operations on clinical studies to ensure client and corporate goals are met, including quality, timelines, and budgetary milestones.
Oversees development and review of study-specific start-up data management documents, including Data Management Plan, Case Report Form Review Guidelines, Editing Specifications, eCRF Completion Manual, Remote Data Entry Instructions, and paper Case Report Forms and/or e-CRF mocks.
Participates in the testing of study-specific data entry packages, both EDC and paper-based.
Provides clarification for edit check development.
Provides clarification for mapping of import data.
Provides review and approval of study-specific EDC packages.
Conducts training of end-users on study-specific EDC package, inclusive of documentation.
Develops and maintains study-specific documentation throughout the lifetime of the project which details QDS’ data operations in accordance with SOPs and GCPs, and the study-specific Scope of Services.
Ensures accurate and timely review of clinical data for errors, omissions, or inconsistencies. Ensures query generation and response application is accurate.
REQUIREMENTS:
Bachelor Degree in health/life sciences preferred or equivalent theoretical/technical depth.
Minimum of 3 years data management experience with at least one year in a CRO environment.
Working knowledge of SAS and SQL as well as knowledge of FDA/ICH guidelines.
Competitive salary.
Local candidates preferred.
Must be able to work unrestricted in the US.
No agencies.
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POSITION: CLINICAL SAS PROGRAMMER
Quality Data Services, Inc. is seeking a contract SAS Programmer with potential for permanent placement.
RESPONSIBLITIES:
Provide statistical programming expertise in the production of analyses, tabulations, graphics, and listings from clinical trial data.
Contribute to the preparation of analysis plans.
Prepare, document, and test required programs and procedures data displays in an efficient manner for inclusion in integrated clinical, statistical reports and other similar documents.
Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming and reporting.
Perform quality assurance procedures on work performed by others.
Develop, test, validate, document, maintain, and execute software and/or systems using the currently endorsed tools or support of production activities.
REQUIREMENTS:
Bachelor Degree in Statistics or a related field. Master's preferred.
Minimum of 3 years SAS programming with at least one year experience in a CRO environment.
CDISC (SDTM/ADaM) experience as well as knowledge of FDA/ICH guidelines.
Competitive salary.
Local candidates preferred.
Must be able to work unrestricted in the US.
No agencies.
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