Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result. Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens. Analyze specimens using approved testing procedures. Review and release test results. Follow CLIA, HIPAA, OSH

The Medical Technologist is responsible for performing clinical laboratory testing which require independent thought and judgment. Responsible for the testing and assessment of blood products and ensures that all testing is completed in a correct and timely manner; follows established policies and procedures to ensure the highest quality of laboratory results; Responsible

t o learn more about the comprehensive benefits program GSK offers US employees. Why Us? GSK is a global biopharma company with a special purpose to unite science, technology and talent to get ahead of disease together so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns as an organization where people can

Site Name UK Hertfordshire Stevenage, USA Pennsylvania Upper Providence Posted Date Apr 12 2024 Are you energized by the opportunity to partner with key leaders in global medical science to accelerate business performance across and drive global operational support? If so, this Clinical Development Director opportunity could be an ideal opportunity to explore. We are seek

t o learn more about the comprehensive benefits program GSK offers US employees. Why Us? GSK is a global biopharma company with a special purpose to unite science, technology and talent to get ahead of disease together so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns as an organization where people can

Site Name USA Pennsylvania Upper Providence, UK London Brentford Posted Date Apr 25 2024 GSK site preferred locations Upper Providence, PA. UK GSK House. On site presence of 2 3 days per week average is anticipated. Additional flexible arrangements considered on case by case basis. As a Director of Patient Centered Outcomes (PCO) you will apply technical expertise to plan

Site Name USA Pennsylvania Upper Providence, Switzerland Zug, UK London Brentford Posted Date May 9 2024 The Director, Oncology Publications will lead the establishment of a Strategic Publication Plan in alignment with Global Medical Plans, medical/scientific communication strategy and objectives. In addition, the Global Oncology Publications Director will ensure that spe

Site Name Washington DC, USA Delaware Dover , USA Delaware Wilmington, USA Maryland Baltimore, USA New Jersey Newark, USA New Jersey New Jersey City, USA Ohio Cleveland, USA Ohio Columbus , USA Ohio Dayton, USA Pennsylvania Philadelphia, USA Pennsylvania Pittsburgh, USA Virginia Richmond, USA West Virginia Charleston , USA West Virginia Morgantown Posted Date May 13 2024

Site Name USA Pennsylvania Philadelphia, Home Worker USA Posted Date May 14 2024 As the Director, Medical Communications and Scientific Training you will be responsible for leading the development of US Vaccines medical communication assets and create scientific communication plans, tactics, field medical educational material and external tools in alignment with the US Me

At The GIANT Company, we are passionate about building strong families and healthy communities, serving millions of neighbors across Pennsylvania, Maryland, Virginia, and West Virginia. We are committed to being an inclusive place to work and shop. Our shared values of care, courage, integrity, teamwork, and humor guide our work as we embrace the unique talents and differ

At The GIANT Company, we are passionate about building strong families and healthy communities, serving millions of neighbors across Pennsylvania, Maryland, Virginia, and West Virginia. We are committed to being an inclusive place to work and shop. Our shared values of care, courage, integrity, teamwork, and humor guide our work as we embrace the unique talents and differ

Adhere to an IRB approved protocol Participate in the informed consent process of study subjects Support the safety of clinical research patients/research participants Coordinate protocol related research procedures, study visits, and follow up care Screen, recruit and enroll patients/research participants Maintain study source documents Under the supervision of PI Report

Works with the research enterprise to locate funding opportunities compatible with the University's research strengths and strategic research objectives. Establishes processes and procedures for effective funding opportunities and provides analyses of funding communications. Identifies submission funding and award opportunities, coordinates applications and reviews, strat

PI240494409

Conducts research assessments on study participants. Assists with and adheres to Institutional Review Board (IRB) renewal, modification, and approved protocols. Assists with training staff. Ensures adherence to protocols and corrects issues with data collection. Essential Functions The Clinical Research Coordinator II performs recruitment of patients and healthy human res