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Job Field: Government Jobs
Location: Travis AFB, CA
Salary: $Not stated

JOB SUMMARY:

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<tr><td valign="top" width="450"><b>Job Title Clinical Research AssistantJob ID Number 204564Company General Dynamics Information TechnologyLocation Travis AFB, CAJob Category EngineeringJob Description As a trusted systems integrator for more than 50 years, General Dynamics Information Technology provides information technology (IT), systems engineering, professional services and simulation and training to customers in the defense, federal civilian government, health, homeland security, intelligence, state and local government and commercial sectors. With approximately 24,000 professionals worldwide, the company delivers IT enterprise solutions, manages large-scale, mission-critical IT programs and provides mission support services. General Dynamics Information Technology is an Equal Employment Opportunity and Affirmative Action employer.**This position is contingent upon contract award.**1. Provide administrative support to the research department to include the collection, compilation and documentation ofclinical research data, in accordance with the details outlined in the research protocol (procedure) for a given study.2. Participate in the recruitment and informed consent of subjects using procedures outlined in the research protocol.3. Assure compliance of general and study specific regulatory processes across multiple studies ofdifferent therapeutic areas and phases.4. Coordinate and implement procedures to collect data from patient medical records; interviews, questionnaires, diagnostic tests and other sources; coordinate with the Laboratory to schedule research subjects for blood draws, cultures, tissues and other specimens for analysis.5. Ensure all activities related to the conduct of this research are in compliance with the details outlined in the research protocol; identify problems and/or inconsistencies and monitor research subjects'' progress to include documentation and reporting of adverse events; recommend corrective action as appropriate.6. Collect clinical data and code as appropriate; prepare oral presentations or written reports setting forth progress, trends and appropriate recommendations or conclusions. Confer with the Principal Investigator and/or the Associate Investigator(s) listed in the research protocol, to assist in the interpretation of the results and manuscript preparation.7. Responsible for completing and submitting protocol related documents to the Wilford Hall IRB, track and maintain annual IRB approval, amendments to the research design and safety events, process requests for information and ensure resolution, maintain Curriculum Vitae(s), Human Subject Research Protection training, and annual Human Subject Research Protection training.Bachelor''s Degree in related scientific field.0-2 years of related scientific experience.1. Must have current Human Subject Research Protection training or be able to acquire it shortly after award.2. Must have current Basic Life Support (BLS) certification.3. Proficiency with Windows based computer programs including Microsoft Office and the ability to conduct data entry in Access, Excel or related databases.4. Must be competent in organizational and communication skills in order to maintain documents and communicate effectively with clinical staff and patients.5. Familiarity and/or experience in a research environment preferred but not required.Apply Online Directly with General Dynamics Information Technology

KEY REQUIREMENTS:

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