Healthcare & Pharma Careers

LocumJobsOnline is working with AAS Locum Tenens to find a qualified Family Practice NP in Houston, Texas, 77003!. About The Position We are seeking an experienced Locums Nurse Practitioner to join a primary care practice that serves patients of all ages in a value-based care setting.. This role offers a flexible schedule and requires autonomous practice in a fast-paced, patient-centered environment.. Embark on exciting adventures and explore new destinations while fulfilling your professional obligations, combining work with leisure and discovery.. Embrace remote work options in telemedicine or virtual healthcare settings, leveraging technology to deliver care from anywhere while maintaining professional engagement.

Outsourcing is not just a method of gaining a one-time cost advantage, but an effective strategy for gaining and maintaining competitive advantages when executed as part of an overall sourcing strategy.. This TPM will work to ensure that the implementation outcomes support requirements and meet targets for quality and UAT, training and user adoption, and for reporting and compliance, particularly in relation to Medicare/DSNP services in California.. Experience with Project Management Information Systems and IT tracking (e.g., Wrike, Azure DevOps, PlanView).. Experience with business and technical solutions in Medicaid and/or Medicare systems, claims, enrollment, provider payments, healthcare analytics, EHR systems, and data management.. Our services include business and technology consulting, data and artificial intelligence, industry solutions, as well as the development, implementation and management of applications, infrastructure, and connectivity.

Position SummaryThe Patient Safety Specialist is responsible for investigating, reviewing and analyzing risk management events, assisting with proactive risk assessment and other patient safety initiatives and education.. The Patient Safety Specialist assists the Director of Risk Management with operational functions of the risk management program.. Support Patient Experience department with Complaint and Grievance responses specific to harm (and potential for liability).. Flexibility with schedule Required Licensure/Certification SkillsCertified Professional in Healthcare Risk Management (CPHRM), Associate in Risk Management (ARM), or Certified Professional Patient Safety (CPPS).. Supervision ReceivedPosition reports to the MFA Director of Clinical Risk Management.

A trusted provider of high quality-home care services is seeking a dedicated and compassionate Home Care Intake Coordinator to join their team.. Coordinate with clinical teams to ensure a smooth transition from hospital or facility to home care.. Ensure compliance with all relevant regulations including insurance authorizations, Medicaid and other funding sources.. Knowledge of homecare ,Medicaid, Medicare, and other insurance programs is a plus.. Proficient in Microsoft Office Suite and electronic health records (EHR)systems.

TNT Healthcare Billing Solutions is seeking a dedicated and detail-oriented Medical Biller to manage full-cycle revenue operations for medical clinics throughout the Twin Cities.. The ideal candidate will possess in-depth knowledge of medical billing, coding, insurance claims processing, and revenue cycle management.. - Review medical documentation and accurately assign appropriate codes using ICD-10, CPT, and HCPCS code sets.. - Ensure compliance with coding and billing regulations, including HIPAA and relevant billing standards.. - Strong knowledge of medical billing procedures, coding systems (ICD-10, CPT, HCPCS), and insurance regulations.

The BIDMC Clinical Research Center serves as a dedicated research unit at BIDMC, supporting ambulatory and overnight research activity.. The Clinical Research Center (CRC) provides the staff, environment and resources to carry out medical research studies for investigators in all clinical disciplines at BIDMC. The CRC is a resource to investigators providing excellent clinical research nursing, specialized testing, a research bionutrition program, and clinical research coordination assistance.. The staff of the Clinical Research Center use a collaborative practice model designed to respond to the care requirements of the CRC patient population, which currently range from late adolescents to frail elders.. Training, evaluation and competencies for this role are overseen by a Nurse Leader to the department.. Employees in this job must be competent to provide patient care to the following age groups: Neonatal:Birth to 6 months, Young adult: 16-30 years, Middle Age: 30 - 60 years, Elderly: 60 -.

The incumbent is accountable for employee safety and will attend safety and loss-control training, engage in injury prevention, perform accident and injury investigations including conducting root cause analysis, and assist in returning employees to regular duty.. Cultivates Respect: Treats others fairly, embraces and values differences, and contributes to a culture of diversity, inclusion, empowerment and cooperation.. Demonstrates Emotional Intelligence: Exhibits a high level of self-awareness, self-management, other awareness and relationship management.. Conducts themselves in an empathic, appropriate way, with a sense of humor and stimulates a collaborative work environment.. BLS required Education:*Master's Degree or ability to obtain a masters degree within thirty months of placement; *Psychiatric Nursing Certification preferred *A minimum of five years of progressively responsible leadership position(s) required, with at least two years in the Nursing leadership space.

Design, develop, and execute automated test scripts using tools like Selenium and programming languages such as Java, JavaScript, and Python to streamline testing processes.. Participate in SOX compliance and audit activities to support regulatory and organizational requirements.. Proficiency in the following tools is a plus: Agile Accelerator, Postman, MuleSoft, Workbench, and Jira. Proficiency in Selenium and Java/Python-based testing frameworks and tools to create and maintain automated test scripts.. Experience in API testing is required , including the ability to design, execute, and analyze API test cases for functionality, reliability, and performance using tools such as JMeter, Postman, and SOA Test. Experience working within Agile Software Development Life Cycle (SDLC) methodologies is required.. Experience testing Salesforce or other CPQ Tool transformations and/or Data Transformation projects strongly preferred.

Provide training regarding service documentation to direct care staff.. QUALIFICATIONS: Education, Experience, and CompetenciesEducation: Master’s degree in counseling, psychology, social work or related field.. Experience and Competencies: Position requires knowledge and experience with electronic health records.. While performing the duties of this job, the employee is occasionally required to stand; walk; sit; use hands to finger, handle, or feel objects tools, or controls; reach with hands and arms, climb stairs or steep and/or rough terrain; balance; stoop, kneel, or crouch; talk or hear; taste or smell.. Masters Degree in Human Services i.e. Counseling, Psychology, Social Work or related field.

The Insurance Patient Account Representative is an extension of a client’s business office staff.. This position will be on a hybrid schedule working two days in the Lewisville, TX office and three days from home.. Appeals & Denials. Guidehouse offers a comprehensive, total rewards package that includes competitive compensation and a flexible benefits package that reflects our commitment to creating a diverse and supportive workplace.. Corporate Sponsored Events & Community Outreach

Clinical Research Coordinator - Cardiology/ arrhythmia / digital health/ lifestyle. The Clinical Research Coordinator (CRC) will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.. Within the Division are sub-specialty sections for: Adult Congenital Heart Disease; Advanced Heart Failure, Transplant, and Pulmonary Hypertension; Cardiac Electrophysiology; Critical Care Cardiology; Cardio-Oncology and Immunology; Echocardiography and Cardiac Imaging; General Cardiology, Interventional Cardiology; and Prevention.. In addition, the Division has significant and complex financial and administrative relationships with the Department of Medicine (DOM) and the UCSF Medical Center, as well as large patient care programs in the sections noted above, large clinical, Federal, and privately supported research programs and six faculty laboratories.. Knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following: Access, Stata, SASS/SPSS, and Teleform programming platforms.

The UNC Lineberger Comprehensive Cancer Center (LCCC) oversees and coordinates oncology clinical trial research for the UNC School of Medicine and UNC Cancer Care. The UNC Lineberger Sponsored Clinical Research team is primarily responsible for the clinical development, regulatory strategic management and FDA interactions for these LCCC sponsored trials.. This position will collaborate in writing, editing, producing and reviewing clinical and/or translational oncology clinical trials protocols.. Required Qualifications, Competencies, and Experience Advanced clinical health science degree MSN, NP, MD) or PhD. Possess excellent written and oral communication skills, interpersonal skills, and be comfortable interacting with individuals at all levels internal and external to UNC Lineberger.. Have a strong record of experience in medical writing or protocol writing and working knowledge of the following: federal and local regulations of clinical trials; drug development; and bio statistics.. Preferred Qualifications, Competencies, and Experience Experience and expertise in oncology research is highly desirable.

Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the U.S. (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma Canada, Inc.) and Europe (Sumitomo Pharma Switzerland GmbH) focused on addressing patient needs in oncology, urology, women's health, rare diseases, psychiatry & neurology, and cell & gene therapies.. We are seeking an experienced VP Clinical Development, Oncology to fulfill a critical and highly visible role to help shape the future of development at SMPA. This role is responsible for the successful strategic positioning and tactical advancement of the clinical programs, and liaises with Clinical (including Clinical Operations), Biometrics, Regulatory, Early Clinical Development, Pre-clinical research, Medical Affairs and Commercial functions.. Provide clinical and medical expertise across all stages of drug development, from preclinical transition to post-marketing.. Provide leadership and clinical expertise to the overall development organization including the clinical development, clinical operations, biometrics, clinical pharmacology, and non-clinical teams.. Prepare and present clinical data to regulatory agencies (FDA, EMA) during IND submissions, clinical study reports, and NDA/MAA filings.

Job Overview: The Clinical Patient Safety Manager plays a vital role in fostering a culture of safety within a healthcare facility.. Reporting to the Director of Risk Management, this position involves creating and maintaining systems to improve patient safety.. Key Responsibilities: - Monitor and evaluate patient safety data to identify trends and opportunities for improvement.. - Investigate patient safety incidents and recommend corrective actions.. - Active California Fire and Life Safety Card (within 30 days of hire).

We apply our expertise to trials at all stages-from early development through approval-with embedded experience in oncology and rare disease.. Spending time to identify leads, qualifying targeted sponsors in the fields of oncology, rare disease, neurology and central nervous system, conducting introductory and follow up meetings with prospective clients, securing RFPs and working with the Business Operations/Proposal Team and other staff as applicable to create proposals for new business. Strategically coordinating members of the Leadership Team to leverage their respective areas of expertise to successfully bring in new business for the company and finding innovative ways to work across business units to effectively sell PMG services.. Ability to drive and availability for domestic and international travel including overnight stays. Experience in oncology, rare disease, neurology, central nervous system

We are seeking a dynamic and experienced Regional Director of Clinical Reimbursement to lead and oversee multiple nursing home facilities.. Conduct regular audits and reviews to ensure accurate documentation, coding, and billing practices.. Professional development opportunities and continuing education support.. The opportunity to make a meaningful difference in the lives of our residents and their families Qualifications: Bachelor's degree in Healthcare Administration, Finance, or a related field.. Knowledge of electronic health records and billing systems.

As a Clinic Research Assistant you will perform day-to-day non-clinical pharmacy operations, administrative activities; Ensures efficient pharmacy workflow and a positive patient experience.. Operations Responsiblies Responsible for assisting pharmacist in the delivery of patient care including patient registration, prescription data entry, preparation of medications for patients, counting, and verifying (where allowed by law).. At the direction of the Pharmacy Manager or pharmacist, prepares, and files reports and records required by the company and various government agencies.. Manages core pharmacy workflow and drives excellence in pharmacy operations.. Manages Community Outreach Portal and coordinates and, at the direction of the Pharmacy Manager, assigns pharmacists to off-site immunization clinics and community events.

Assist BMS attorneys and the Attorney General’s office in compiling evidence for litigation preparation.. Draft Document Desk Review decisions on behalf of the Commissioner to affirm or reverse denials.. Oversee claims payments, prior authorization processes, reconsideration requests, and denials.. Process Freedom of Information Act (FOIA) requests, gather responsive documents from BMS staff, prepare materials for legal review, and compile final correspondence.. Access and navigate multiple systems—including KEPRO C3, KEPRO C3 Nursing Homes, QNXT, ISIGHT, AD HOC Reports Manager, Health PAS, Health PAS-Rx, and Review Manager (INTERQUAL Criteria)—to analyze and audit claims, prior authorization requests, member hearing requests, and provider denials.

Looking for an experienced, motivated, and "can do" Assistant Director of Nursing(ADON/ADNS) for our Newton location.. As the ADON/ADNS, you are the second in command of the nursing department.. You will work closely with the DON/DNS to improve the quality of patient care and services provided by your team in our 45 bed SNF or Memory Care Unit. In their absence, you will oversee the entire team, ensuring quality customer service and compliance with all federal, state, and local rules and regulations, as well as the policies and procedures set by your employer.. Qualifications IncludeMust have a current unencumbered Registered or Licensed Practical Nurse license in the stateMinimum of 3 years supervisory experience in long term careStrong knowledge of Medicare/Medicaid/Joint Commission guidelines requiredMust be computer literate.. Knowledge of EMR required COVID-19 Precaution(s)Kindly submit your resume for immediate consideration today!

Join Takeda as a Director, Immunotherapy/ Immuno-Oncology, In Vitro Pharmacology where you will play a major role in the discovery of novel biologics, contributing to the strategic direction of our immunotherapy/ immune-oncology research programs.. Provide strategic direction and leadership for the Immunotherapy and Immuno-oncology in vitro pharmacology team, ensuring alignment with company goals and objectives.. Lead the Immunotherapy and Immuno-oncology biologics discovery programs with cross-functional teams, driving the programs from lead ID to preclinical development.. Minimum of 10 years of experience in Immunotherapy/immuno-oncology research, with a focus on immune cell biology, immune checkpoints, and tumor-immune interactions.. Proven track record of leading successful in vitro pharmacology efforts in the field of immunotherapy/immuno-oncology, including assay development and validation, candidates screening, and mechanism of action studies.