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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, modeling our val
Posted 1 day ago
Pfizer
- Groton, CT / South San Francisco, CA / Collegeville, PA / 59 more...
Accountable for managing overall study timelines, budgets and quality targets Accountable for building, forecasting and managing the Clinical Trial Budget Leads the core study team; manages, facilitates and documents core study team meetings (e.g. meeting agendas & minutes, action logs and decision logs) and facilitates effective decision making Ensures adequate study team resources and leads stud
Posted Today
Waters Corporation
- Milford, MA / Virginia Beach, VA / Philadelphia, PA / 3 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
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 8 days ago
Novartis is recruiting for a Medical Science Liaison to cover MD, DC, VA. Preferred location is DC. A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented, performance driven people. All of which makes us one of the most rewarding employers in our field. We're committed to pe
Posted 11 days ago
The Oncology Representative/Specialist/Senior Specialist will be responsible for representing and promoting Novartis Pharmaceuticals Corporation as a leader in the Oncology community and marketplace. As one of the largest pharmaceutical companies in the world and a pioneer in Oncology, we are committed to peak performance, improving the quality of life, and embracing and leveraging diverse backgro
Posted 11 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 12 days ago
Covance
- San Diego, CA / Gaithersburg, MD / Greenfield, IN
, you’ll be empowered to own your career journey with mentoring, training and personalized development planning. Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow’s drug development challenges, creating new possibilities for our clients—and your career. We are presently hiring a Client Services Manager for our San Diego, CA, Greenfield, IN or Ga
Posted Today
Senior PMO Analyst , Clinical Research (Finance/Operations) Job Location(s) US VA Chantilly Job Number 2017 14669 Job Category Finance Position Type Full Time Job Overview Covance Senior PMO Analyst Play a pivotal role in the drug development process and grow your career Are you interested in making an impact through your everyday work? Would you enjoy working in a team focused environment as you
Posted Today
Pfizer
- Groton, CT / Peapack, NJ / Madison, NJ / 22 more...
The Senior Medical Writer collaborates with members of the clinical study team to author protocols and independently interprets study results to prepare high quality clinical study reports (CSRs), public disclosure synopses (PDS) and related clinical documents within agreed upon timelines. Responsibilities Collaborates with clinicians, statisticians and clinical scientists to author protocols. Ind
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 8 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 12 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 8 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 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 11 days ago
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