43 Results for

Clinical Research Coordinator Jobs in Kansas City, MO

Jobs

Kansas City, MO30+ days ago

Responsible for performing diverse administrative and clinical responsibilities requiring some analysis, sound judgment, and a high level of knowledge of specific research study protocols, Good Clinical Practice Guidelines, Federal research regulations, and institutional requirements. Responsible for coordination and management of clinical study protocols and along with the research investigator, manages many aspects of the clinical trial and conducts all research activities within an ethically based framework in accordance with federal, state, and local regulations.

Kansas City, MO10 days ago

$70,200–$105,300 Per Year

The SCRC collaborates with investigators, sponsors, and research staff to facilitate study conduct, contributes to study budgets and regulatory submissions, participates in quality assurance activities, and provides guidance to Clinical Research Coordinators as needed.

Job Description Summary:

The Senior Clinical Research Coordinator (SCRC) in the Department of Pediatrics manages clinical research studies by overseeing complex activities related to the collection, documentation, and analysis of research data in accordance with regulatory requirements and institutional policies.

Kansas City, MO30+ days ago

$60,800–$91,200 Per Year

p>Job Description Summary:

The Clinical Research Coordinator in the Department of Internal Medicine, Division of Nephrology works collaboratively with multidisciplinary teams, research, and hospital staff to recruit, screen, educate, and assist in the kidney transplant clinical research studies. Additionally, the Clinical Research Coordinator monitors participant progress, documents and reports adverse events, and participates in periodic quality assurance audits of study protocols.

Kansas City, MO24 days ago

$60,800–$91,200 Per Year

Job Description Summary: The Clinical Research Coordinator in the department of Cardiology works collaboratively with multidisciplinary teams, research, and hospital staff in the overall clinical study coordination of clinical research. Participate in quality assurance activities by reviewing clinical data in medical record charts, assessing pharmacy compliance with protocol criteria and reviewing study documentation to ensure compliance with GCP guidelines and FDA CFR.

KS26 days ago

$60,800–$91,200 Per Year

Job Description Summary: Job Description: The Clinical Research Coordinator works collaboratively with multidisciplinary teams, research, and hospital staff to recruit, screen, educate, and assist in the overall clinical study coordination of clinical research. Assist with study specific excel spread-sheet type protocol eligibility, demographics, evaluability and biomarker results summary to assist PI in monitoring study progression as well as gathering data for interim PMRC assessments and/ or presentations.

Overland Park, KS10 days ago

Provide/coordinate the highest level of contact, counseling and support services Coordinate study activities and patient care with medical staff · Implement and adhere to study protocol · Perform Phlebotomy and IV procedures · Prepare laboratory specimens for analysis, monitoring tests and procedures, shipping frozen specimen · Execute medical orders within parameters of education, training and licensure · Conduct study activities helping to ensure all safety parameters · Maintain patient records in EMR and appropriate hospital records · Assess and report adverse study events, including the IRB and any research sponsors · Complete all paperwork affiliated with the study, including but not limited to the requirements of the facility, the IRB and the study Sponsor. · Assess each proposed study protocol · Facilitate administrative review and approval of proposed studies · Develop tactical study procedures · Develop any necessary study documents not provided by sponsor or IRB · Educate HCA staff regarding research and study protocols · Screen and recruit patients based on protocol criteria · Explain study protocols, procedures and treatments to patients and families · Conduct the Informed Consent process in conjunction with study investigators · Ensure that an original copy of any subjects Informed Consent Document is the in the research binders, as well as, a copy on the subject's medical record.

KS30+ days ago

$70,200–$105,300 Per Year

p>Job Description Summary:

The Senior Clinical Research Coordinator works collaboratively with multidisciplinary teams, research, and hospital staff to recruit, screen, educate, and assist in the overall clinical study coordination of clinical research. The Senior Clinical Research Coordinator will manage assigned clinical research studies by supervising a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data.

Kansas City, MO30+ days ago

$60,800–$91,200 Per Year

The position works directly with research participants and assists with regulatory, operational, and data‑related aspects of clinical research, as well as activities related to liver specimen biobanking and distribution. Job Description Summary: The Clinical Research Coordinator in the Department of Internal Medicine, Division of Gastroenterology and Liver Center supports clinical and translational research activities.

KS30+ days ago

$60,800–$91,200 Per Year

p>Job Description Summary:

The Clinical Research Coordinator works collaboratively with multidisciplinary teams, research, and hospital staff to recruit, screen, educate, and assist in the overall clinical study coordination of clinical research.

Participate in quality assurance activities by reviewing clinical data in medical record charts, assessing pharmacy compliance with protocol criteria and reviewing study documentation to ensure compliance with GCP guidelines and FDA CFR.

Fairway, KS30+ days ago

$60,800–$91,200 Per Year

li>

Assists physician in cerebrospinal fluid (CSF) collection for clinical trials by educating patient / caregiver regarding the lumbar puncture procedure, preparing lumbar puncture supplies, providing supplies to physician during procedure while maintaining sterile field, aliquoting CSF by protocol-specified amounts into separate vials for storage and transport, instructing patient/caregiver in post-lumbar puncture care and expectations, conducting follow -up phone call to determine if any adverse events were experienced.

Coordinates of all aspects of study visit activities for patients and families, including scheduling of hospital-based procedures such as MRI and PET, and other procedures to include clinical study visit interviews and assessments, ECG, lab draws, IV infusions, lumbar punctures, and dispensation of study medication.

New!

Overland Park, Kansas3 days ago

p>To provide clinical research support for studies involving human subjects including administration; project implementation, meeting support, quality assurance, and dissemination of results, recruitment; collection, recording, and editing of interview, questionnaire, and clinical data; performing quality assurance monitoring of study data; randomization of study participants; conducting case management tasks; scheduling participant appointments; supporting clinical and group intervention; review medical records following study protocols; and performing other duties in support of clinical trials services as assigned.

Provide assistance in the administrative, technical and scientific day-to-day operation of the study to assure project goals and timelines are met, quality data is collected and managed, and to assure participant and/or data confidentiality.

Kansas City, MO30+ days ago

As a Clinical Research Coordinator in this position, you will prepare the site for conduct of the study identify potential study participants, conduct informed consent, assist with scheduling labs and appointments, gather and record study related data, and provide patient education for various research studies. Saint Luke's Hospital in Kansas City, MO is seeking a Research Coordinator to join our research team to assist with providing and coordinating care for patients active in various research studies.

Kansas City, MO30+ days ago

Scheduling subjects for study visits and conducts appointment reminders; Building/updating source as needed; Conducting monitoring visits and resolves issues as needed in a timely manner; Ensuring study related reports and patient results are reviewed by investigator in a timely manner; Filing SAE/Deviation reports to Sponsor and IRB as needed; Documenting and reporting adverse events; Reporting non-compliance to appropriate staff in timely manner; Maintaining positive and effective communication with clients and team members; Always practicing ALCOAC principles with all documentation; May assist with study recruitment, patient enrollment, and tracking as needed; Maintaining confidentiality of patients, customers and company information, and; Performing all other duties as requested or assigned. Responsibilities may include but are not limited to: Screening of patients for study enrollment; Patient consents; Patient follow-up visits; Documenting in source clinic charts; Entering data in EDC and answers queries; Obtaining vital signs and ECGs; May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Requesting and tracking medical record requests; Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies;].

New!

Overland Park, KS4 days ago

Overland Park, KS7 days ago

p>SUMMARY:

To provide clinical research support for studies involving human subjects including administration; project implementation, meeting support, quality assurance, and dissemination of results, recruitment; collection, recording, and editing of interview, questionnaire, and clinical data; performing quality assurance monitoring of study data; randomization of study participants; conducting case management tasks; scheduling participant appointments; supporting clinical and group intervention; review medical records following study protocols; and performing other duties in support of clinical trials services as assigned.

ESSENTIAL DUTIES AND RESPONSIBILITIES.

Provide assistance in the administrative, technical and scientific day-to-day operation of the study to assure project goals and timelines are met, quality data is collected and managed, and to assure participant and/or data confidentiality.

Overland Park, KS7 days ago

p>SUMMARY:

ESSENTIAL DUTIES AND RESPONSIBILITIES.

Provide assistance in the administrative, technical and scientific day-to-day operation of the study to assure project goals and timelines are met, quality data is collected and managed, and to assure participant and/or data confidentiality.

Kansas city, Missouri30+ days ago

li>Scheduling subjects for study visits and conducts appointment reminders;

Building/updating source as needed;

Conducting monitoring visits and resolves issues as needed in a timely manner;

Ensuring study related reports and patient results are reviewed by investigator in a timely manner;

Filing SAE/Deviation reports to Sponsor and IRB as needed;

Documenting and reporting adverse events;

Reporting non-compliance to appropriate staff in timely manner;

Maintaining positive and effective communication with clients and team members;

Always practicing ALCOAC principles with all documentation;

May assist with study recruitment, patient enrollment, and tracking as needed;

Maintaining confidentiality of patients, customers and company information, and;

Performing all other duties as requested or assigned. Responsibilities may include but are not limited to:

Screening of patients for study enrollment;
Patient consents;
Patient follow-up visits;
Documenting in source clinic charts;
Entering data in EDC and answers queries;
Obtaining vital signs and ECGs;
May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
Requesting and tracking medical record requests;
Updating and maintaining logs, chart filings;
Maintaining & ordering study specific supplies;].

Kansas City, MO10 days ago

$60,800–$91,200 Per Year

p>Job Description Summary:

The Clinical Research Coordinator in the Department of Pediatrics collaborates with multidisciplinary teams, research personnel, and site staff (e.g., clinics, hospitals, and other pediatric sites) to support clinical research. https://www.kumc.edu/human-resources/benefits.html.

KS28 days ago

$70,200–$105,300 Per Year

The position provides professional nursing care and patient monitoring for clinical trials and works collaboratively with multidisciplinary teams, research personnel, and hospital staff to recruit, screen, educate, and support participants throughout the clinical study coordination process. Job Description Summary: The Clinical Research Nurse Coordinator in the Cancer Center manages clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data.

Kansas City, MO24 days ago

$28.20–$38.35 Per Hour

Certifications: Research certification such as: Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP) or Association of Clinical Research Professionals (ACRP). At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above.

Kansas City, KS30+ days ago

$28.20–$38.35 Per Hour

p>The University of Kansas Cancer Center (KUCC) is the region''s only National Cancer Institute-designated cancer center where patients gain access to the most promising therapies, cutting-edge clinical trials and world class research. The CDC is responsible for working collaboratively with the Research Nurse Clinician, Clinical Research Coordinator and Clinical Lab Coordinator in the coordination and collection of data for cancer clinical trials.

Overland Park, KS10 days ago

With a focus on meeting the needs of our patients at all access points, Physician Services is dedicated to implementing innovative, physician-driven, value-added solutions to assist physicians in providing high-quality, patient-centered care, aligning with our mission to care for and enhance human life. Supporting HCA Healthcare's 186 hospitals and 2,400+ sites of care, Physician Services plays a crucial role as the main entry point for patients looking for high-quality healthcare within the HCA Healthcare system.

Kansas City, KS30+ days ago

$60,800–$91,200 Per Year

p>Job Description Summary:

The Clinical Research Coordinator (CRC) in the Division of Pulmonary, Critical Care, and Sleep Medicine is responsible for coordinating and managing clinical research studies in accordance with regulatory requirements and institutional policies. The CRC will collaborate with investigators, sponsors, and participants to facilitate all aspects of study conduct, including subject recruitment, informed consent, data collection, and reporting.

MO14 days ago

Remote

$60,036.16–$78,047.01 Per Year

Our approach is rooted in a "grow our own" philosophy, designed to help our team members build meaningful, long-term careers with us, supported by benefits that make a real difference, including:

Career growth and development opportunities, with clear pathways and ongoing support.
Baptist Health is the region''s largest not-for-profit healthcare organization, with 12 hospitals, over 29,000 employees, 4,500 physicians and 200 outpatient centers, urgent care facilities and physician practices across Miami-Dade, Monroe, Broward and Palm Beach counties.

Overland Park, KS30+ days ago

$62,300–$195,100 Per Year

p>Excellent interpersonal skills, able to establish rapport with a wide range of people Business experience a plus Customer service skills Excellent technology and administrative skills Excellent presentation skills Strong oral and written communication skills in local language Demonstrated ability to complete patient recruitment activities including referral outreach, chart reviews, and data abstraction Demonstrated ability to execute tasks with minimal oversight Demonated ability to coordinate and complete activities across multiple functions Able to work independently - candidates should be self-motivated Frequent travel up to 75%, with potential for overnight stays.

Competencies:

• Demonstrated analytical skills • Demonstrated Business Acumen • Demonstrated success in persuasion, influence, and negotiation skills • Demonstrated leadership ability • Demonstrated ability to apply technical/scientific knowledge • Flexibility to learn new products over time • Knowledge of and experience with the selling process • Initiative & execution-oriented.

Kansas City, MO30+ days ago

$60,800–$91,200 Per Year

p>Job Description:

Job Duties:

• Manage and perform activities related to multiple areas of sponsored projects administration, including but not limited to pre-award and post-award activities for multiple cost centers. • Support grant opportunities, facilitate proposal development, contribute to non-technical components of proposals, process proposals, develop budgets, support contract development, and ensure compliance with laws, regulations, policies, and terms and conditions.

Kansas City, MO30+ days ago

$33.75–$50.63 Per Hour

li>

Perform study defined procedures and assessments, including, but not limited to, vital signs, IV placement, drug administration, lab collection, lab processing, phlebotomy, electrocardiograms, etc. in strict compliance with the study protocol. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above.

MO19 days ago

ul>

Must qualify as a General Medical Laboratory Scientist under CLIA-88 through one of the following: Bachelor's degree in a chemical, physical, biological, clinical laboratory, or medical technology science field; or actively enrolled in an accredited Medical Laboratory Scientist program, OR Associate degree in a laboratory science or medical laboratory scientist program, OR Previously qualified or eligible to qualify as a generalist prior to February 29, 1992 under 42 CFR 493.1427 (3/14/90).

In this dynamic role, you'll partner with investigators, research coordinators, laboratory staff, and healthcare professionals to support innovative research that helps shape the future of medicine.

MO13 days ago

$134,000–$190,000 Per Year

p>What you will need (Required):

Bachelor's Degree and a minimum of 5 years clinician experience in intra-operative procedures acquired from Registered Nursing Degree curriculum (RN), or in positions such as Radiologic Technologist (RT), Operating Room Technician (ORT), or Cardiovascular Technician (RCIS) or related medical device, clinical, or Certification in RDCS (Registered Diagnostic Cardiac Sonographer) within ARDMS (American Registry for Diagnostic Medical Sonography) OR equivalent experience based on Edwards criteria.
Represent the Clinical Affairs Research Team during clinical trial cases with investigating physicians, hospital staff and clinical research coordinators by providing on-site, real-time guidance during clinical trial implants, including contingency planning to address unforeseen occurrences in support of assigned clinical investigations.

KS19 days ago

Remote

$97,000–$193,000 Per Year

li>

Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded.

As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.

Shawnee, KS30+ days ago

p>Our Clinical Research Associates add value through the following responsibilities:

Coordinates and conducts GCP and study protocol training at study sites and assures training is documented Builds rapport with study site staff to assure compliance with the protocol, applicable regulatory and guidance documents, SOPs, and all study activities Assists in reviewing the study records and all study notebooks to ensure contents are current and complete Assists in providing tracking and Quality Control (QC) of data as required and assists with responses to QA audits Evaluates Investigators and assists with selection of appropriate sites to conduct clinical studies Collaborates with the study Project Manager to assure study sites selected meet the needs of the study protocol Monitors assigned study sites through review of electronic data capture (EDC) systems, faxed, emailed, and paper documentation. Serves as the liaison between Argenta US Clinical and study site personnel Facilitates clarifications, corrections, and data query resolution with study sites or data management personnel Tracks adverse events (AE's) encountered in clinical studies and ensures all serious AEs and non-serious AEs are documented and communicated appropriately to the Project Manager and Sponsor Learns to assist with facilitates clarifications, corrections, and data query resolution with study sites or data management personnel.

Kansas City, MO30+ days ago

As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Kansas City, MO21 days ago

$111,521–$144,981 Per Year

Intimate Partner Violence Assistance Program Coordinator (IPVAP-C) is a Social Work Program Coordinator who will provide clinical evidence-based services including assessments and interventions; program development; Veteran, family, Caregiver and staff education on domestic violence and intimate partner violence; community outreach; resource development; continuous quality improvement activities; and evaluation/consultation. The Department of Veterans Affairs performs pre-employment reference checks as an assessment method used in the hiring process to verify information provided by a candidate (e.g., on resume or during interview or hiring process); gain additional knowledge regarding a candidates abilities; and assist a hiring manager with making a final selection for a position.

KS30+ days ago

Remote

li>

Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.

New!

Kansas City, MO6 days ago

The Division of Hematology/Oncology/Bone Marrow Transplantation at Children’s Mercy Kansas City is seeking a full-time BE/BC Pediatric Hematologist/Oncologist to join our Oncology Team with a focus in the care of children and adolescents with hematologic malignancies. Inpatients are overseen by 4 Hem/Onc services – an inpatient resident/fellow H/O team, a chemotherapy team, BMT team, and an inpatient coagulation consultation team – all staffed by residents and/or advanced practice professionals.

New!

Kansas City, MO6 days ago

Kansas City, Missouri30+ days ago

Overview:

KS30+ days ago

Remote

$80,000–$90,000 Per Year

Responsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.

Excelsior Springs, MO30+ days ago

$107,456–$167,188 Per Year

A Doctoral degree in any area of psychology and, in addition, successfully complete a re-specialization program (including documentation of an approved internship completed as part of the re-specialization program) meeting both of the following conditions: The re-specialization program must be completed in an APA or a CPA accredited doctoral program; and. Applicants who have a doctoral degree awarded between 1951 and 1978 from a regionally accredited institution with a dissertation primarily psychological in nature may fulfill this internship requirement by having the equivalent of a one-year supervised internship experience in a site specifically acceptable to the candidates doctoral program.

Kansas City, MO30+ days ago

$80,600–$120,900 Per Year

p>Job Description Summary:

The Clinical Research Supervisor supports the All of Us Research Program Heartland Consortium at the University of Kansas Medical Center by leading and contributing to enrollment, engagement, and data collection of pediatric and adult research participants.

Monitor and drive progress toward enrollment targets, including approximately 700 pediatric participants annually, and implement strategies to address gaps.

New!

Kansas City, MOToday

Kansas City, MO30+ days ago

p>Ultimately, Saint Luke's Cancer Institute in partnership with the Marion Bloch Neuroscience Institute aims to be recognized nationally as a center known for:

High-quality, compassionate neuro-oncology care Strong clinical trial enrollment and innovation Multidisciplinary excellence Leadership in programmatic growth and outcomes. The director will provide clinical leadership, oversee existing brain tumor clinical trials, and develop new investigator-initiated studies and industry collaborations to broaden therapeutic options for patients.

New!

Kansas City, MO6 days ago

Kansas City is large enough to provide the features of a metropolitan area, but still allows for easy commutes, assessable amenities and a very high quality of life with highly ranked public schools, great parks and other green spaces, and lots of amazing people. Building on a busy clinical program and growing research profile, the Division Director will advance the academic growth of the faculty, recruit aspiring investigators and foster an environment that encourages world class clinical care and new discoveries that advance the field.

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Clinical Research Coordinator Jobs in Kansas City, MO

Clinical Research Coordinator - Women''''s Health Department University Health.

Senior Clinical Research Coordinator - Pediatrics University of Kansas Medical Center

Clinical Research Coordinator - Internal Medicine (Nephrology) University of Kansas Medical Center

Clinical Research Coordinator- Cardiology University of Kansas Medical Center

Clinical Research Coordinator (Breast Cancer Prevention) Cancer Center University of Kansas Medical Center

Clinical Research Coordinator HCA Healthcare Inc

Senior Clinical Research Coordinator - Cancer Center University of Kansas Medical Center

Clinical Research Coordinator - Internal Medicine (Gastroenterology) University of Kansas Medical Center

Clinical Research Coordinator - Cancer Center University of Kansas Medical Center

Clinical Research Coordinator - Neurology (Neuromuscular) University of Kansas Medical Center

Clinical Research Coordinator - Must be local to Overland Park, KS! Stiles Eyecare Excellence

Clinical Research Coordinator Saint Luke's Health System Inc

Clinical Research Coordinator Alcanza Clinical Research LLC

Clinical Research Coordinator - Must be local to Overland Park, KS! Eye Care Partners Career Opportunities

Clinical Research Coordinator - Must be local to Overland Park, KS! EyeCare Partners LLC

Clinical Research Coordinator - Must be local to Overland Park, KS! Stiles Eyecare Excellence & Glaucoma Institute

Clinical Research Coordinator Alcanza Clinical Research

Clinical Research Coordinator - Pediatrics University of Kansas Medical Center

Clinical Research Nurse Coordinator University of Kansas Medical Center

Clinical Data Coordinator- Cardiology University of Kansas Medical Center

Clinical Data Coordinator (North Comm Site) Cancer Center University of Kansas Medical Center

Registered Nurse Clinical Research HCA Healthcare Inc

Clinical Research Coordinator - Internal Medicine (Pulmonary, Critical Care, and Sleep Medicine) University of Kansas Medical Center

MCI Hybrid Quality Assurance Specialist 2, Research Administration, FT, 9A-5:30P Baptist Health South Florida Inc

Clinical Trial Educator - Registered Nurse IQVIA Holdings Inc

Budget Analyst - Comprehensive Integrated Research Operations University of Kansas Medical Center

Clinical Research Nurse PRN - CTSU University of Kansas Medical Center

Clinical Research Lab Technician - Internal Medicine Research University Health.

Senior Specialist, Clinical Education THV AR (MidWest US) Edwards Lifesciences Corp

Senior Clinical Research Associate - Oncology - Central - Remote Worldwide Clinical Trials Holdings Inc

Animal Health Clinical Research Associate III Argenta Ltd

Clinical Research Associate II ICON Plc

Social Worker - Intimate Partner Violence Assistance Program Coordinator U.S. Department of Veterans Affairs

Senior Clinical Research Associate ICON Plc

Pediatric Hematologist/Oncologist Children's Mercy Hospital (MO)

Pediatric Oncologist Children's Mercy Hospital (MO)

Pediatric Oncologist Children's Mercy KC

Oncology Monitoring Excellence Academy - OMEA Fortrea Inc

Staff Psychologist - Mental Health Clinic BHIP U.S. Department of Veterans Affairs

Clinical Research Supervisor - Internal Medicine (All of Us Research Program) University of Kansas Medical Center

Physician Urology - Competitive Salary Source Medical, LLC.

Medical Director of Neuro-Oncology - Saint Luke''''s - Kansas City Saint Luke's Health System Inc

Division Director – Neurology Children's Mercy Hospital (MO)

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