Healthcare & Pharma Careers

Compliance & Quality Assurance Engineer. Develop, review and accept Quality Assurance Plans (SQAP/HPAP) to ensure certification compliance. Quality Assurance Plans (SQAP/HPAP).

Perks & Benefits At Froedtert Health Froedtert Health Offers a variety of perks & benefits to staff, depending on your role you may be eligible for the following: Paid time off Growth opportunity- Career Pathways & Career Tuition Assistance, CEU opportunities Academic Partnership with the Medical

If you are currently employed at Smithfield, please log into Workday and submit your application through the Jobs Hub.A great job-and a great future-awaits you at Smithfield Foods.We are an American food company with a leading position in packaged m.

Coordinate the day-to-day administrative activities of the clinical research trials program. The Medical College of Wisconsin (MCW) is an Equal Opportunity Employer. Assure compliance with all relevant IRB and other regulatory agency requirements.

Perform the day-to-day administrative activities of clinical research trial programs. Outstanding Healthcare Coverage, including but not limited to Health, Vision, and Dental. The Medical College of Wisconsin (MCW) is an Equal Opportunity Employer.

Apply knowledge of clinical research to provide recommendations and direction to clinical research teams to ensure budgetary compliance throughout all phases of the Clinical Trial Financials Lifecycle. The Clinical Trial Budget Specialist II will coordinate the day-to-day study-related activities of

SummaryUnder general supervision the Clinical Research Quality Assurance Specialist II is responsible for the oversight of clinical research study protocols of increasing complexity, with an emphasis on quality, training, monitoring, and the development of tools for study team use. Apply knowledge o

Coordinate research related projects such as mailings, participant contact information, patient visits and focus groupsCollect samples from patients as needed. Code and enter onto clinical research forms and into computerized database. SummaryAssist study coordinators by providing administrative and

Under general supervision the Clinical Research Quality Assurance Specialist II is responsible for the oversight of clinical research study protocols of increasing complexity, with an emphasis on quality, training, monitoring, and the development of tools for study team use. Apply knowledge of clini

Baxter Healthcare in Round Lake, Illinois is seeking a Documentation Specialist to support manufacturing operations through critical documentation review. You will ensure compliance with Good Manufacturing Practices, assisting in the accuracy and completeness of records essential for product release

Administrative Assistant to support clinical research studies. Responsibilities include coordinating patient visits, maintaining study participant files, collecting and entering data, and supporting patient enrollment in educational studies. The Medical College of Wisconsin, Inc.

The Medical College of Wisconsin seeks a dedicated individual to assist study coordinators by providing vital administrative and data collection support for clinical research studies. The role involves conducting research activities, coordinating patient visits, and managing study documents while en

Perform the day-to-day administrative activities of the clinical research trials program. Clinical Research Trials Program Administrator. Assist in the evaluation and writing of research protocols.

Organize study participant charts and files, and distribute to appropriate locationCollect required data from study coordinators and research nurses, and enter onto clinical research forms and into computerized databaseVerify accuracy of bills and stipendsGenerate letters to be sent to study partici

Perform the day-to-day administrative activities of clinical research trial programs. Collect, analyze, and disseminate research data. Data utilization, complex problem solving, critical thinking, resource management, and writing skills.

Froedtert Health is hiring for a position focused on improving patient safety across multiple clinics in Wisconsin. The role requires collaboration with hospital leaders and clinical staff to enhance care practices and processes.

This position offers a chance to gain practical experience in a controlled environment while ensuring compliance with safety requirements. The Medical College of Wisconsin seeks students for laboratory roles focused on drug development and efficacy. The ideal candidate is pursuing studies in pharmac

Code and enter onto clinical research forms and into computerized database. Summary Assist study coordinators by providing administrative and data collection support for clinical research studies. Coordinate research related projects such as mailings, participant contact information, patient visits