1. PATIENT SAFETY Follows established hospital and departmental precautions and procedures in the performance of all job duties to ensure a safe work environment for patients and others to include as appropriate Demonstrates appropriate hand hygiene Demonstrates use of two patient identifiers Demonstrates effective communication "hand offs" between providers, shifts, depa

We're offering a generous sign on bonus to welcome you to our team. Recognizing and valuing exceptional talent, we're eager to discuss the exciting details of this bonus during our interview process. Full Time 40 hours. Overnight shift 11pm 7 am M F alternating weekends and Holidays In a highly regulated environment (AABB, CAP, TJC, DPH, CMS), performs critical functions

1. Oversight of the clinical trials start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. 2. Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolutio

1. Leadership a. Provide direction and guidance to pharmacist and ancillary support including technician staff in following policy and procedure, taking accountability and ownership of job responsibilities, and promoting professional behavior and attitudes. b. Provide feedback to the pharmacy managers/practice managers/medical directors for the interim and annual performa

Per Diem Medical Laboratory Scientist Generalist Chemistry/Hematology/Coag/UA/Rapid Microbiology and Planting. Phlebotomy.EKG. BS in Medical Laboratory Science, ASCP preferred. Qualifications BS Medical Laboratory Scientist, ASCP preferred Primary Location MA Boston MEI Mass Eye and Ear Main Building Boston Work Locations MEI Mass Eye and Ear Main Building Boston 243 Char

1. Recruits, screens, and enrolls eligible patients with chronic liver disease for study participation in both inpatient units and outpatient clinics 2. Performs data collection through various methods including interviews and surveys with patients, caregivers, and clinicians 3. Opportunities for performing data analysis to publish in peer review research journals and pre

Please note, the functions below are representative of major duties that are typically associated with these positions. Specific responsibilities may vary based upon departmental needs. Similarly, not all duties that have been outlined will be assigned to each position. Coordinate research and administrative activities, ensuring all projects and tasks are completed accord

As it pertains to the service area in the pharmacy department, responsible for the optimization of drug therapy by identification, resolution, and prevention of drug related problems and improving therapeutic outcomes. Responsible for providing direct or indirect patient care according to the laws and regulations governing pharmacists and the practice of pharmacy by the a

Pharmacy Practice Involvement Proactively maintain proficiency in the skills and theory of the practice of pharmacy by reviewing literature, attending in services, seminars, and conferences. Actively participate in clinical meetings Participate in training staff as directed Cross train for other roles to provide periodic support as directed based on business needs Partici

Come join our team and play a pivotal role in promoting and ensuring an environment where human subject research is conducted according to the highest standards! Our Team Our Human Research Affairs Compliance and Education Office was established in June 1999 as the Quality Assurance/ Quality Improvement (QA/QI) Program within the Office of Human Research Affairs at Mass G

Provides certified Epic build expertise and experience for successful product implementation Provides certified Epic design expertise to analyze organization's current business practices and translate them into configurations and workflows Supports departmental/ functional team with application and information system knowledge Completes specific tasks as directed. Tracks

The Clinical Research Coordinator (CRC) will provide support for research activities in the Metabolic Bone Diseases Unit. Reporting to the Principal Investigator, the CRC will assist with recruitment, assessment and follow up in research studies. Responsibilities Responsible for participant recruitment, assessment and follow up for a cohort study Provide back up support f

Do you want to work at one of the top 100 hospitals in the nation? ChristianaCare is currently recruiting for a Clinical Pharmacist to join our team. Life is full of choices, and ChristianaCare recognizes whom you work for is an important decision. Choose an organization that values pharmacy services and provides the opportunity to impact the health of our community adher

Accountable for dispensing medications in the hospital in accordance with the physician's patient care plan, established departmental and hospital policies, and legal requirements. Interpret and screen physician orders for appropriate dosage, route of administration, drug or therapeutic incompatibilities, and contradictions with subsequent resolution of any questions aris

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting opera