Principal Investigator Salary at Pacarctic Llc BETA

CICONIX is HIRING an Administrative Human Subjects Protection Scientist to support the Institutional Review Board (IRB) of the Headquarters of the Office of Human and Animal Research Oversight (OHARO), Office of Human Research Oversight (OHRO) at the US Army Medical Research and Development Command (MRDC). The OHARO OHRO is responsible for ensuring that USAMRDC conducts, contracts, sponsors, supports or manages research, and U.S. Army Medical Command investigations involving human subjects, human anatomical substances or animals are conducted in accordance with Federal, DoD, Army, USAMRDC, and international regulatory requirements. The HSP AS contractor shall provide excellent and timely customer service and support to his/her HRPO Team staff, HRPO Approval Authority, Principal Investigators, and other HRPO customers. Administrative support includes preparing official correspondence related to management of a protocol from the time of its submission to the HRPO until the protocol file’

Job Details Level Experienced Job Location VHA: Washington DC - Washington, DC, WA Position Type Full Time Job Shift Day Description What makes Brillient a GREAT fit for you? When you join Brillient, you become part of an award-winning Full Spectrum Digital Transformation company focused on helping agencies in the continuum of analog, to digital, to analytics, leading to insight-driven decision making and mission execution. Our mission is to provide value to our clients and our people, operate with the highest integrity as a trusted business partner, adopt a workstyle that is flexible allowing us to effectively collaborate while being agile and nimble, and be innovative in everything we do. We are passionate about ensuring our employees experience a work environment that is inclusive, professional, and supportive. In addition to these core values, the Brillient team is driven by: •Focus on Sustainability- Being an environmentally conscious, green company with sustainable practices. •Im

General Summary of Position The Nurse Practitioner or Physician Assistant will be responsible for providing medical management to research subjects enrolled in designated studies. The Nurse Practitioner (NP) will participate in several research studies, as the medical liaison and sb or co-investigator/coordinator as appropriate. The NP is responsible for assessment, screening, diagnosis, evaluation, and monitoring the general management plan, and follow up assessment and intervention for clinical research participants and/or patients. This position, under the general Scientific Director or designee will function independently and in collaboration with MCCRC Physicians and Principal Investigators. Primary Duties and Responsibilities Contributes to the achievement of established department goals and objectives and adheres to department policies, procedures, quality standards, and safety standards. Complies with governmental and accreditation regulations. Consistently demonstrates support

Posting Details I. DEPARTMENT INFORMATION Job Description Summary: Founded in 1824, the GW School of Medicine and Health Sciences (SMHS) is the 11th oldest medical school in the country and the first in the nation's capital. Since its establishment, the school has been at the forefront of medical education and has grown to include highly-ranked programs in the health and biomedical sciences. With dozens of top-tier residency programs, SMHS is a competitive and esteemed destination for medical school graduates across the country. Find out more here: http://smhs.gwu.edu/. The Department of Biochemistry and Molecular Medicine (BMM) of the George Washington University, School of Medicine and Health Sciences (SMHS), strives to deliver the highest quality of professional education and training, and conduct cutting-edge research in the areas of biochemistry, molecular genetics, and genomics with a goal to better understand human disease. Additionally, the Department continues to have a long a

Overview: Contract (Expected to go though the end of the year) Full-time M-F (Standard business hours) Medical Device Study POSITION SUMMARY: The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Clinical Research Manager, the Principal Investigator and the Medical Director. The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials. The CRC will perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study specific protocols. Duties and Responsibilities: Administratively and clinically manage an average of six to eight clinical trials Adhere to Research SOP’s Adhere to Good Clinical Practices and the study protocols Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials Discuss study protocols with patients

This position requires extensive experience in molecular biology, cell biology, immunology and genetics. The position requires the ability to integrate these disciplines in performing laboratory experiments in animal models and in cell culture. Qualifications: Minimum Education Doctor of Philosophy (Ph.D.) (Required) Functional Accountabilities Responsible Conduct of Research Consistently demonstrates adherence to the standards for the responsible conduct of research. Plans, conducts and manages research projects within federal and institutional regulations and policies under the direction of the principal investigator. Uses research funds and resources appropriately. Maintains confidentiality of data as required. Meets all annual job-related training and compliance requirements. Laboratory Work Performs routine and non-routine tests as directed and required by specific research program. Records and checks results for completeness and accuracy. Performs tasks that may require familiari

The Opportunity: We are seeking a detail-oriented, proactive, critical thinker to manage and review workers' comp claims as a Claims Examiner. As a Claims Examiner, your duties will include investigating and processing insurance claims, negotiating settlements, and maintaining accurate claims records. The ideal candidate should have a strong understanding of worker's compensation policies and regulations, excellent investigative skills, and exceptional customer service skills. If you have no prior experience with these policies and regulations, you must be willing to learn and be responsible for implementing claims based on these policies and regulations. Responsibilities: Learn/understand worker’s compensation policies and regulations. Review workers' compensation claim forms. Assists claimants as needed in relating their claim. Assists management with more complex cases. Maintains accurate records and prepares required reports on all cases. Performs other related duties as assigned.

Description As the proliferation of digital systems continues to transform all aspects of society, our national security increasingly relies on our mastery of electronic warfare (EW). The Leidos Advanced Warfare Technology division in Arlington, VA is searching for a Software Engineer Team Lead. This role combines team lead and hands-on software engineering responsibilities. Key Responsibilities: • Team Lead (approximately 30% of the time): Supervise and lead a team of approximately four software engineers supporting multiple projects as part of a larger software engineering branch. This includes performance reviews, time card approval, managing coverage of their direct reports, mentoring, interfacing with program managers, retention, and recruiting. • Software Engineer (approximately 70% of the time): Contribute to software design, development, and test of advanced systems as a part of multi-disciplinary teams. Teams include signal processing, firmware, hardware, systems engineering,