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POSITION SUMMARY The Senior Director, Government Affairs and Policy (GA&P) is a high profile, high impact, senior leadership position, and a member of the US Commercial Leadership Team. The Senior Director is responsible for all federal legislative, reimbursement and advocacy strategy and execution for facets of Avanir's business. These areas of responsibility affect all aspects of the business in
Posted Today
Waters Corporation
- Washington, DC / Virginia Beach, VA / Philadelphia, PA / 1 more...
Perform on site customer training on Waters' LC/MS instrumentation and software MS application and method development support for customers who have purchased on site applications assistance Perform training courses on MS instrumentation and software for customers and in house staff (including engineers and other service support staff) as necessary Develop and maintain technical expertise on Water
Posted Today
Waters Corporation
- Charlotte, NC / Philadelphia, PA / Baltimore, MD / 3 more...
Aggressively develop new prospects and penetrate competitive accounts while maintaining current customer base for assigned market Perform solution based selling to meet or exceed sales targets Implement strategic sales initiatives into the district that are consistent with corporate goals and objectives Keep current on assigned market dynamics, application trends, and competitive information Manag
Posted Today
This position will act as a Clinical Research Ethicist, providing expertise on the implementation of relevant Human Subjects Protection regulations in clinical research. Responsibilities include Conducting regulatory and bioethical reviews of clinical trial protocols, including domestic and international sample and site specific informed consent documents, for compliance with applicable federal re
Posted 9 days ago
Follow batch production records (BPRs) and SOPs for GMP/GTP manufacture of tissue products. Utilize good documentation practices. Assist in the preparation of reports and other documentation as applicable to the scope of operations in the manufacturing facility. Identify areas for improvement in manufacturing efficiencies and compliance. Assist with technology transfer from R&D to manufacturing en
Posted Today
Manage and process SAEs; assist in the preparation of reports; generate specified data reports from the database; process and review investigator safety reports and notifications for non IND adverse event reports; process and review safety narratives for IND and non IND Adverse Event cases as required; maintain electronic files for the department; and query SAE databases. Requirements Requirements
Posted 9 days ago
The Alaka`ina Foundation Family of Companies (FOCs) is comprised of industry recognized government service firms designated as Native Hawaiian Organization (NHO) owned and 8(a) certified businesses. The Family of Companies (FOCs) includes Ke`aki Technologies, Laulima Government Solutions, Kupono Government Services, and Kapili Services. Alaka`ina Foundation activities under the 501(c)3 principally
Posted 13 days ago
Incumbent will serve in myriad capacities as a senior scientist/engineer, subject matter expert, principal investigator, system architect, technical lead, task lead or program manager focused on the research, development, and fielding of CBRNE signature collection, analysis or exploitation sensor or forensic science technologies, methods and services. Incumbent must work collaboratively with colle
Posted 7 days ago
The Safety and Pharmacovigilance Specialist will perform various tasks in support of clinical research including adverse event analysis and processing, serious adverse event reconciliation, preparation of IND safety reports for submission to the FDA, safety document or data analysis, and clinical trial site support. . Requirements M.D. from a U.S. accredited institution with active U.S. medical
Posted 9 days ago
Description of Responsibilities The primary responsibility of this individual is to review and inspect US and international clinical research and clinical trial sites engaged by USAMRIID, Division of Medicine. The secondary responsibility of this individual will be to assist with clinical research efforts at USAMRIID, including, but not limited to, management of a clinical sample repository. Tasks
Posted 13 days ago
CVS Health
- District Heights, MD
Job Description Summary Health is everything. At CVS Health, colleagues are committed to increasing access, lowering costs and improving quality of care. Millions of times a day, we help people on their path to better health from advising on prescriptions to helping manage chronic and specialty conditions. As a Staff Pharmacist, you have a critical role at the forefront of delivering our purpose,
Posted 6 days ago
This position will act as a Clinical Research Ethicist, providing expertise on the implementation of relevant Human Subjects Protection regulations in clinical research.Responsibilities include conducting regulatory and bioethical reviews of clinical trial protocols, including domestic and international sample and site specific informed consent documents, for compliance with applicable federal reg
Posted 14 days ago
Seek funding from DTRA and other funding agencies on behalf of the Government and USAMRIID to further the research portfolio of the Division and USAMRIID. Establish and coordinate extramural collaborations and contracts to augment the research program he or she directs. Amount of funding per year will vary depending on current mission requirements and USAMRIID’s available funding. Coordinate
Posted 14 days ago
This position will require preparing scientific and regulatory documents (e.g. clinical protocols, investigator's brochures, informed consent forms, annual reports, investigational new drug applications, new drug applications, regulatory correspondence, and clinical summary reports). Must have the ability to prepare investigator/pharmaceutical company meeting minutes, analyze preclinical and clini
Posted 14 days ago
Field Identification of Biological Warfare Agents
Posted 14 days ago
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