Qureos Mentor

ABSS SOLUTIONS, INC

<p></p><div><div>ABSS Solutions, Inc. (ASI), is seeking a full-time Senior Clinical Research Coordinator to join our team in providing Medical Research support to the 59th Medical Wing in San Antonio, Texas. ASI administers a comprehensive research and development contract providing an array of research projects for customers across the DoW space. Our research teams work with educational institutions and other third party organizations to maximize readiness, and resilience for the men and women of our armed forces.</div><div></div><p><br>
Duties &amp; Responsibilities:</p><ul><li>
Supports Government directors, PIs, in the planning, programming, and execution of clinical research projects and protocols and associated activities.</li><li>
Maintain study records related to participation in accordance with protocols, study schedules, participant observation, and provides follow up documentation to the PI.</li><li>
Coordinates multiple, concurrent projects for the PI/director; confers with investigator on experimental design; provides instruction on various research laboratory techniques, and study participant contact procedures.</li><li>
Organize research information; manages reporting and data collection.</li><li>
Monitors comprehensive research study budgets.</li><li>
Research equipment/supply catalogs, and recommend purchase requests for projects/protocols in accordance with the IRB.</li><li>
Documents all regulatory research and administrative actions needed for study compliance.</li><li>
Prepares/delivers required reports and other research documentation to PI.</li><li>
Prepares correspondence, creates and maintains study files, develop study schedules, and presentation graphics to support the research study.</li><li>
May require occasional weekend and evening hours.</li></ul><p>
Minimum Qualification and Experience:</p><ul><li><b>
Required</b>: B.S in Biological Sciences; Masters highly preferred.</li><li><b>
Required</b>: Experience coordinating and managing clinical research studies involving <b>human subjects</b>.</li><li><b>
Required</b>: Experience ensuring compliance with all <b>regulatory</b> requirements in clinical research, including FDA regulations, Good Clinical Practice (GCP) guidelines, institutional policies, and IRB requirements.</li><li>
5-8 years&rsquo; minimum experience in clinical research.</li><li>
Preferred candidate will hold a current certification, such as Certified Clinical Research Coordinator (CCRC).</li><li>
Demonstrated competence in oral and written communication.</li><li>
Demonstrated experience managing multiple concurrent clinical projects (5+ years).</li><li>
Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor.</li><li>
Intermediate+ experience with Microsoft Office applications including: Word, Excel, PowerPoint, Outlook, Access, Publisher, and SharePoint.</li><li>
Intermediate+ experience with Adobe Acrobat and internet applications.</li><li>
Experience in use of computerized information systems related to Human Subjects Research required (i.e. eIRB or related software).</li><li>
Successful completion and maintenance of Human Subjects training / training in human subjects' research protection, bioethics, and HIPAA.</li></ul></div><p></p>

Senior Clinical Research Coordinator

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ABSS SOLUTIONS, INC

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Senior Clinical Research Coordinator