23 pharmacy jobs found

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Responsible for unit dose distribution including familiarity with medications, dosage forms and storage requirements. May also compound sterile and non-sterile medication preparations. Communicates with pharmacists and nursing staff to ensure timely preparation and delivery of medications. Delivers medications, including controlled substances, to nursing areas and ancillary departments in accordance with established policies and procedures, and DEA and DPH regulations. Job Description: Essential Responsibilities: 1. Restocks automated dispensing machines (ADSs) and floor stock medications. Follows relevant Epic workflows including but not limited to loading medications, dispensing doses, dispense tracking, and fulfilling cart fill items.  2. Delivers all medication in compliance with all DEA, DPH & State Board of Pharmacy regulations. 3....

The Pharmacy Department at the Dana-Farber Cancer Institute places emphasis on the values of reliability, professionalism, cooperation, teamwork, communication, positivity and inclusiveness. The Pharmacy Technician I, Research is responsible for providing technical support to research pharmacy operations under the supervision of a licensed pharmacist. Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers,...

The Pharmacy Department at the Dana-Farber Cancer Institute places emphasis on the values of reliability, professionalism, cooperation, teamwork, communication, positivity and inclusiveness. The Pharmacy Technician I, Research is responsible for providing technical support to research pharmacy operations under the supervision of a licensed pharmacist. Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers,...

The Pharmacy Department at the Dana-Farber Cancer Institute places emphasis on the values of reliability, professionalism, cooperation, teamwork, communication, positivity and inclusiveness. The Pharmacy Technician II, Research is responsible for providing technical support to research pharmacy operations under the supervision of a licensed pharmacist. The Pharmacy Technician II, Research will staff in pharmacy locations/areas as required. Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that...

Location: Avera Research Institute-Sioux Falls Worker Type: Regular Work Shift: Day Shift (United States of America) Pay Range: The pay range for this position is listed below. Actual pay rate dependent upon experience. $20.75 - $36.50 Position Highlights This position may support multiple types of research projects at Avera Research Institute, including observational studies and clinical trials. Research areas may include maternal and child health, public health, clinical research, and other studies involving varied patient populations across multiple health conditions.    This position may include supporting the ECHO study, Environmental influences on Child Health Outcomes, a longitudinal, observational study following pregnant women and their children to better understand how environmental exposures during the prenatal and early childhood time frame affect health outcomes for children later in life.   The position may also support clinical...

The Clinical Research Coordinator (CRC) will work within the Breast Oncology clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Research Manager. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely facilitation of trial assessments per protocol and collection of protocol related samples including shipment to outside entities as required. Will support and maintain participant/subject trial binders and may maintain regulatory binders, to ensure study compliance with all state, federal, and IRB requirements. May be responsible for pertinent IRB protocol submissions. This individual may also screen patients for protocol eligibility, obtain informed consent for non-treatment trials, and register study participants with the...

Hello, Thank you for your interest in career opportunities with the University of Mississippi Medical Center.  Please review the following instructions prior to submitting your job application: Provide all of your employment history, education, and licenses/certifications/registrations.  You will be unable to modify your application after you have submitted it. You must meet all of the job requirements at the time of submitting the application.  You can only apply one time to a job requisition.  Once you start the application process you cannot save your work. Please ensure you have all required attachment(s) available to complete your application before you begin the process. Applications must be submitted prior to the close of the recruitment. Once recruitment has closed, applications will no longer be accepted. After you apply, we will review your qualifications and contact you if your application is among the most highly qualified. Due to the...

Location: Sioux Falls, SD Worker Type: Regular Work Shift: Day Shift (United States of America) At Avera Heart Hospital, you’re not just joining a workplace – you’re becoming part of a family. With more than 700 dedicated employee, we deliver care that truly makes a difference. Our commitment to excellence has earned us the distinction of being one of only a handful of hospitals nationwide – out of more than 4,000 – to achieve a double 5-star rating from the Centers for Medicare and Medicaid Services. Position Highlights A brief overview Works under the general direction of cardiovascular research leadership and in collaboration with principal investigators, research nurses, coordinators, physicians, advanced practice providers, and operational teams. Supports high-quality clinical research involving cardiovascular devices, medications, heart failure, structural and interventional cardiology, electrophysiology, vascular care, prevention, and other heart and...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Job Description: This position operates within a multidisciplinary team to support clinical research from implementation of a protocol/trial, to patient support, through active data monitoring. -Collaborates with local hematology/oncology physicians, nurses, pharmacy, office support staff as well as other research members across the BILH network t stay up to date with new and ongoing oncology research and operations -Assists investigators to meet the needs defined by particular studies -Works alongside providers to recruit and consent patients to various trials -Provides both supportive and direct patient care to those who enroll to a trial including scheduling collaboration, symptom monitoring and maintenance, and follow up care/monitoring -Acts as an active member on all multidisciplinary tumor boards and department committees Clinical resource...

The Department of Family and Community Medicine at the Medical College of Wisconsin (MCW), seeks a board certified / board eligible physician to lead our research within the department**.** Candidates will also support clinical care by seeing patients in the residency programs. This position is located in Milwaukee, WI at the Medical College of Wisconsin. We are comprised of nationally and internationally renowned, dedicated group of faculty and staff with a strong commitment to clinical care. Position Highlights: Evolve the research operation so eventually it consistently achieves target Blue Ridge ranking, brings in research funds from other sources and broadly supports research into questions of importance to primary care, family medicine, and underserved or minority populations. Participate as a member of the DFCM Executive Team led by the Department Chair Sustain robust lines of research and funding, develop new lines of research and funding while attracting new...

The Medical College of Wisconsin’s Department of Pathology and Laboratory Medicine is seeking an academically oriented faculty member to join the Cytogenetics and Molecular Pathology team at a rank that is commensurate with experience. Position Highlights: We are seeking a highly motivated individual who will help lead the molecular diagnostics and cytogenetics. Will collaborate with clinical colleagues in Pathology as well as with the community at Froedtert and the Medical College of Wisconsin. Help enhance the utilization of precision medicine assays to improve population health and wellness in the patients seeking care at Froedtert and the Medical College of Wisconsin. Academic rank and salary will be commensurate with experience. Provide authoritative interpretation and sign-out of complex clinical molecular genetic and cytogenetic testing (including chromosome analysis and FISH) for oncology and inherited disorders within a high-volume, academically...

The CRC (Clinical Research Coordinators) work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Research Manager. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely facilitation of trial assessments per protocol and collection of protocol related samples including shipment to outside entities as required. Will support and maintain participant/subject trial binders and may maintain regulatory binders, to ensure study compliance with all state, federal, and IRB requirements. May be responsible for pertinent IRB protocol submissions. This individual may also screen patients for protocol eligibility, obtain informed consent for non-treatment trials, and register study participants with the clinical trials...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. The Clinical Research Coordinator will be responsible for the coordination and administration of multiple research studies. Works closely with principal investigators and research staff facilitating all aspects of assigned clinical trials. Implements study protocols in accordance to regulatory and institutional requirements. Sets up administrative systems to manage the progress of each study while screening, recruiting and following study participants and collecting and reporting study data. Interacts with study participants diagnosed with various medical conditions and diagnoses. Job Description: Essential Duties & Responsibilities including but not limited to:   Completes new coordinator orientation and all required trainings.   Responsible for coordinating different phases of research studies with varying degrees of complexity with moderate...

The Gastrointestinal (GI) Oncology Clinical Research Program at Dana-Farber Cancer Institute is seeking a Clinical Research Coordinator (CRC) to join our program. The GI Oncology Clinical Research Program supports PI initiated, industry sponsored, and cooperative group phase I - IV clinical trials across multiple GI cancers, including esophageal, stomach, liver, pancreas, colon, and neuroendocrine. The Clinical Research Coordinator work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB...

The Clinical Research Coordinator (CRC) will work within the adult Leukemia clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Research Manager. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely facilitation of trial assessments per protocol and collection of protocol related samples including shipment to outside entities as required. Will support and maintain participant/subject trial binders and may maintain regulatory binders, to ensure study compliance with all state, federal, and IRB requirements. May be responsible for pertinent IRB protocol submissions. This individual may also screen patients for protocol eligibility, obtain informed consent for non-treatment trials, and register study participants with the...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Under the direction of the Supervisor of Research Oncology Informatics, the Research Oncology Informatics Pharmacist plays a critical role in supporting the successful implementation of investigational therapies within Epic. This position partners closely with Principal Investigators, Research Nurses, Research Assistants, and other Cancer Clinical Trials Office staff to design, build, and maintain investigational medication records in Willow and treatment plans in Beacon. The pharmacist provides oversight of adult research chemotherapy treatment plans, ensuring accuracy, regulatory compliance, and operational efficiency. Through close collaboration with Hematology/Oncology investigators and research teams, this role helps ensure timely review, approval, and ongoing management of investigational treatment plans, supporting high-quality clinical research and patient...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Under the direction of the Supervisor of Research Oncology Informatics, the Research Oncology Informatics Pharmacist plays a critical role in supporting the successful implementation of investigational therapies within Epic. This position partners closely with Principal Investigators, Research Nurses, Research Assistants, and other Cancer Clinical Trials Office staff to design, build, and maintain investigational medication records in Willow and treatment plans in Beacon. The pharmacist provides oversight of adult research chemotherapy treatment plans, ensuring accuracy, regulatory compliance, and operational efficiency. Through close collaboration with Hematology/Oncology investigators and research teams, this role helps ensure timely review, approval, and ongoing management of investigational treatment plans, supporting high-quality clinical research and patient...

Hello, Thank you for your interest in career opportunities with the University of Mississippi Medical Center.  Please review the following instructions prior to submitting your job application: Provide all of your employment history, education, and licenses/certifications/registrations.  You will be unable to modify your application after you have submitted it. You must meet all of the job requirements at the time of submitting the application.  You can only apply one time to a job requisition.  Once you start the application process you cannot save your work. Please ensure you have all required attachment(s) available to complete your application before you begin the process. Applications must be submitted prior to the close of the recruitment. Once recruitment has closed, applications will no longer be accepted. After you apply, we will review your qualifications and contact you if your application is among the most highly qualified. Due to the...

Hello, Thank you for your interest in career opportunities with the University of Mississippi Medical Center.  Please review the following instructions prior to submitting your job application: Provide all of your employment history, education, and licenses/certifications/registrations.  You will be unable to modify your application after you have submitted it. You must meet all of the job requirements at the time of submitting the application.  You can only apply one time to a job requisition.  Once you start the application process you cannot save your work. Please ensure you have all required attachment(s) available to complete your application before you begin the process. Applications must be submitted prior to the close of the recruitment. Once recruitment has closed, applications will no longer be accepted. After you apply, we will review your qualifications and contact you if your application is among the most highly qualified. Due to the...

Hello, Thank you for your interest in career opportunities with the University of Mississippi Medical Center.  Please review the following instructions prior to submitting your job application: Provide all of your employment history, education, and licenses/certifications/registrations.  You will be unable to modify your application after you have submitted it. You must meet all of the job requirements at the time of submitting the application.  You can only apply one time to a job requisition.  Once you start the application process you cannot save your work. Please ensure you have all required attachment(s) available to complete your application before you begin the process. Applications must be submitted prior to the close of the recruitment. Once recruitment has closed, applications will no longer be accepted. After you apply, we will review your qualifications and contact you if your application is among the most highly qualified. Due to the...