11 medical office assistant jobs found

Overview The Certified Medical Assistant / Registered Medical Assistant performs routine administrative and patient care support duties in a medical practice to assist medical and/or nursing staff in the examination and treatment of patients and ensures that the office runs smoothly. The CMA/RMA/MA will also be in chart of prior authorizations. The employee is responsible for identifying prior auth requirements by insurance/payer and processes and completes prior authorizations for scheduled and add on services. Determines if services are a covered benefit and documents prior auth information in Epic. Communicates with provider and nurse if services were approved or denied. Facilitates peer to peer reviews when needed. Qualifications Registered Medical Assistant (RMA), American Registry of Medical Assistants (ARMA) Registered Medical Assistant (RMA), American Allied Health (AAH) Certified Medical Assistant (CMA), National Center for Competency Testing (NCCT) Certified...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Under limited supervision of the principal investigator, conducts a variety of routine and specialized laboratory tests using molecular, cell biology and/or biochemistry techniques. Performs lab procedures with speed, precision, and understanding of theory behind tests and procedures. Performs Level II responsibilities with a higher level of problem resolution, analytical ability, self-direction, and expertise. Job Description: Primary Responsibilities: Perform routine and non-routine laboratory tests which may include DNA sequencing, gene cloning, in situ hybridization, immunohistochemistry, northern blotting; synthesizes and interprets results. (essential) May operate and maintain moderate to complex lab equipment such as spectrophotometer, flow cytometer, etc. (essential) Using analytical abilities and sound judgment, makes decisions...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Under supervision of the principal investigator, conducts a variety of routine experiments using molecular, cell biology and/or biochemistry techniques. Records test results, calculates, transcribes, and analyzes data using basic statistics. Job Description: Essential Responsibilities: Conducts routine tests following established procedures, which may include assays, DNA sequencing, tissue culture, protein purification, Southern blotting, PCR analysis, electrophoresis, chromatography. (essential) Researches and collects basic study data through monitoring devices and maintains daily logs/basic records of methodologies and test results. With supervision, using databases, may summarize data and interpret results using descriptive statistics and basic hypothesis testing. (essential) Performs literature searches and library investigations as they...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Under general supervision of the principal investigator, conducts a variety of routine and specialized laboratory tests using molecular, cell biology and/or biochemistry techniques. Performs lab procedures with speed, precision, and understanding of theory behind tests and procedures. Performs Level I responsibilities with a higher level of problem resolution, analytical ability, and self-direction. Job Description: Primary Responsibilities: Performs routine and non-routine laboratory tests which may include DNA sequencing, gene cloning, in situ hybridization, immunohistochemistry, northern blotting; synthesizes and interprets results. (essential) May operate and maintain moderate to complex lab equipment such as spectrophotometer, flow cytometer, etc. (essential) Using analytical abilities and sound judgment, makes decisions regarding the...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. The ideal candidate would have prior expertise with mouse surgery for cortical brain imaging and experience with acquisition of cellular imaging data. The goal would be to join a team exploring cellular activity of molecularly defined neuron types in mouse visual cortex across various brain states, and the state-dependent influences of neuromodulators and peptides (www.andermannlab.com). Job Description: Essential Responsibilities: Conducts routine tests following established procedures, which may include assays, DNA sequencing, tissue culture, protein purification, Southern blotting, PCR analysis, electrophoresis, chromatography. (essential) Researches and collects basic study data through monitoring devices and maintains daily logs/basic records of methodologies and test results. With supervision, using databases, may summarize data and...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Under general supervision of the principal investigator, conducts a variety of routine and specialized laboratory tests using chemistry, molecular, cell biology and/or biochemistry techniques. Performs lab assays, records test results, calculates, transcribes, and analyzes data using basic statistics. Job Description: Essential Responsibilities: Performs routine and non-routine laboratory tests which may include protein assays, chemical derivatization, protein digestion, protein purification, mass spectrometry and interprets results. May operate and maintain moderate to complex lab equipment such as spectrophotometer, flow cytometer, etc. (essential) Using analytical abilities and sound judgment, makes decisions regarding the reliability and accuracy of results, repeating procedures when necessary. (essential) May assist with planning...

The Clinical Research Project Manager I is responsible for the day-to-day coordination and management of clinical trial activities, primarily focusing on multi-center, PI-initiated trials. They ensure trial and site startup coordination, train site research staff, handle regulatory submissions, track safety events, and communicate with regulatory authorities. Reporting to disease group managers and/or Clinical Trials Office (CTO) leadership the Clinical Research Project Manager I identifies project plan variances and develops contingency plans to maintain project milestones. They may also oversee operational and training aspects of the EPIC/OnCore application, working closely with faculty, staff, and stakeholders to develop infrastructure, procedures, and tracking systems for project management services. This role requires independent work under general supervision within their disease group or CTO, with a focus on ensuring compliance and efficient trial execution. Located in...

The Medical University of South Carolina (MUSC) is seeking a faculty physician to join our well-established academic Family Medicine team at assistant, associate, or professor level to provide comprehensive primary care. The ideal candidate will be a patient-centered, compassionate team-player who is invested in delivering state of the art clinical care, while also teaching and leading parts of the curriculum for students and/or residents. Any candidate with an interest in medical education will be highly considered. The department plays a major role in all four years of the medical school curriculum. Our department has a significant presence in the Dean s Office, including the role of dean, associate deans, and curriculum directors. We also play a major role in facilitating different outreach activities to different underserved and vulnerable groups, including people who are unfunded, rural, and/or currently unhoused. The department has a highly successful required core...

The Assistant Clinical Research Manager (ACRM) position will work within the Sarcoma clinical research program and assist in the management of the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. These positions, in collaboration with the program’s Clinical research Managers physicians and research nursing staff, are responsible for assisting with the design, implementation and evaluation of their program’s clinical research activities, related regulatory oversight, and will provide day to day supervision of their program’s clinical research staff as needed. This position’s work location is hybrid with two or three days per week onsite in Boston, MA. The selected candidate may only work remote days from a New England state (ME, VT, NH, MA, CT, RI). Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and...

The Assistant Clinical Research Manager (ACRM) position will work within the Center of Early Detection & Intervention Blood Cancers (CEDI BC) Interventional Clinical Trials clinical research program and assist in the management of the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. These positions, in collaboration with the program’s Clinical research Managers physicians and research nursing staff, are responsible for assisting with the design, implementation and evaluation of their program’s clinical research activities, related regulatory oversight, and will provide day to day supervision of their program’s clinical research staff as needed. This position’s work location is hybrid with two or three days per week onsite/remote. The selected candidate may only work remote days from a New England state (ME, VT, NH, MA, CT, RI). Located in Boston and the surrounding communities, Dana-Farber...

This Assistant Clinical Research Manager (ACRM) position will work within the Breast Oncology clinical research program and assist in the management of the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. These positions, in collaboration with the program’s Clinical research Managers physicians and research nursing staff, are responsible for assisting with the design, implementation and evaluation of their program’s clinical research activities, related regulatory oversight, and will provide day to day supervision of their program’s clinical research staff as needed. 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...