Medical Coordinator Visa Sponsorship Jobs in Kansas
Medical coordinator visa sponsorship jobs in Kansas are concentrated at health systems like The University of Kansas Health System, Stormont Vance in Topeka, and Ascension Via Christi in Wichita. These employers coordinate patient care, insurance authorizations, and care transitions across the state's growing regional medical centers and rural health networks.
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Get Access To All JobsCompany Description
At EVERSANA®, we are proud to be a Great Place to Work across the globe. We’re fueled by our vision to create a healthier world. How? Our global team of more than 6,000 employees is committed to creating and delivering next-generation commercialization services to the life sciences industry. We are grounded in our cultural beliefs and serve more than 670 clients ranging from innovative biotech start-ups to established pharmaceutical companies. Our products, services and solutions help bring innovative therapies to market and support the patients who depend on them. Our jobs, skills and talents are unique, but together we make an impact every day. Join us!
Across our growing organization, we embrace diversity in backgrounds and experiences. Improving patient lives around the world is a priority, and we need people from all backgrounds and swaths of life to help build the future of the healthcare and the life sciences industry. We believe our people make all the difference in cultivating an inclusive culture that embraces our cultural beliefs. We are deliberate and self-reflective about the kind of team and culture we are building. We look for team members that are not only strong in their own aptitudes but also who care deeply about EVERSANA, our people, clients and most importantly, the patients we serve. We are EVERSANA.
Job Description
THE POSITION:
The Medical, Legal and Regulatory (MLR) review is an essential process in healthcare marketing to make sure advertising, promotional and non-promotional content is accurate, compliant, and ready to be published. The MLR process must rigorously control and execute review, approval and document filing actions. As part of the MLR team, the Medical, Legal and Regulatory (MLR) Coordinator is responsible for managing all the MLR processes for a dedicated client. The Medical, Legal and Regulatory (MLR) Coordinator ensures that all administrative and program management support for the client’s MLR process operates effectively and in full compliance with all internal and external policies and regulations.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Our employees are tasked with delivering excellent business results through the efforts of their teams. These results are achieved by:
MEDICAL, LEGAL AND REGULATORY (MLR) COORDINATOR RESPONSIBILITIES
- Manages the end-to-end MLR process.
- Responsible for scheduling, setting the agenda, and leading Review Committee meetings.
- Add live discussion notes for comments discussed in Veeva Vault.
- Scribe meeting minutes, circulate draft meeting minutes for Committee approval and finalize and file approved minutes.
- Ensure all covered communications are properly vetted through the review process utilizing the online review system (e.g., Veeva Vault PromoMats and Vault MedComms).
- Cascade and enforce any new policies and guidelines related to review of materials.
- Verifies that materials are assigned to the appropriate review path. Rejects incomplete submissions and materials that are not review ready. Facilitates/documents discussion in live meetings.
- QCs Final Document vs. Approved Document.
- Supports FDA 2253 submissions, or country specific regulatory submissions with MLR Regulatory Reviewer/Partner.
MEDICAL CONTENT SUPPORT RESPONSIBILITIES
- Support the development of project plans.
- Support medical content development team.
- Support upload of materials into clients’ review and approval platforms, including supporting annotating, anchoring references, etc.
MEDICAL AFFAIRS AND MEDICAL INFORMATION PROJECT MANAGEMENT SUPPORT
- Support Medical Affairs and Medical Information leadership in developing and managing project plans for key initiatives.
- Demonstrate a commitment to diversity, equity, and inclusion through continuous development, modeling inclusive behaviors, and proactively managing bias.
- All other duties as assigned.
Consistent with the Americans with Disabilities Act (ADA) and applicable state and local laws, it is the policy of EVERSANA to provide reasonable accommodation when requested by an employee with a disability, unless such accommodation would cause an undue hardship for EVERSANA. If reasonable accommodation is needed to perform the essential functions of your job position, please contact Human Resources.
EXPECTATIONS OF THE JOB:
- Travel: In general, this position does not travel.
- Hours: Able to work full-time and be flexible with work scheduling as required by clients and management.
- Metrics: Maintain and contribute toward process improvement which positively impacts metrics associated with activities of the MLR Review process; metrics are subject to change annually or more often as deemed necessary.
- Customer Services: Maintain and improve customer services associated with the activity of the MLR review.
- Time Management: Complete MLR coordination responsibilities in a timely manner.
The above list reflects the general details necessary to describe the expectations of the position and shall not be construed as the only expectations that may be assigned for the position.
An individual in this position must be able to successfully perform the expectations listed above.
Qualifications
MINIMUM KNOWLEDGE, SKILLS AND ABILITIES:
The requirements listed below are representative of the experience, education, knowledge, skill and/or abilities required.
- Education: Graduates in any Life Sciences / Biomedical field.
- Must demonstrate excellent ability to communicate effectively in English, both orally and in writing.
- Experience and/or Training:
- At least 2 years of experience in a healthcare agency or pharmaceutical company.
- Experience with use of Veeva Vault PromoMats / MedComms.
- Experience in Scientific Writing / Scientific Reviewing / MLR.
- Project management.
- Time management.
- Meeting management.
- Excellent customer service skills.
- Technology/Equipment: Computer proficiency in Outlook and Microsoft Office Suite (Word, Excel, PowerPoint, and other Window applications).
PREFERRED QUALIFICATIONS:
- Education: Graduates/Postgraduates in Pharmacy or Medicine preferred.
- Experience and/or Training
- Working knowledge of or familiarity with global healthcare compliance statutes and laws.
- Ability to perform assignments with a high degree of independence requiring extensive experience, skill, and knowledge.
- Excellent computer skills including competency in presentation, word processing and spreadsheet software, utilizing MS Office Suite.
- Proven ability to manage multiple tasks, set priorities and meet deadlines.
- Ability to manage cross-functional projects.
- Familiar with laws and regulations regarding US drug/device advertising and promotion, including industry best practices.
- Knowledge of medical terminology (preferred but not required).
- Must be quality-oriented and demonstrate consistent attention to detail.
- Must have the ability to follow established processes and procedures and the flexibility to adopt new practices and priorities as required.
- Positive Attitude and Energy – Exhibits an upbeat attitude, a genuine interest in others and a sense of humor. Energizes others and heightens morale through her/his attitude.
- Communication Skills – Possesses the ability to develop and articulate ideas and information that generate understanding and create a climate that motivates and encourages others to participate.
- Innovator – Transforms creative ideas into original solutions that positively impact the company’s performance.
- Highly Principled – Proves to be a professional of unquestionable integrity, credibility and character who demonstrates high moral and ethical behavior.
PHYSICAL/MENTAL DEMANDS AND WORKING ENVIRONMENT:
The physical and mental requirements along with the work environment characteristics described here are representative of those an individual encounters while performing the essential functions of this position.
Office: While performing the essential functions of this job the employee is frequently required to reach, grasp, stand and/or sit for long periods of time (up to 90% of the shift), walk, talk and hear; occasionally required to lift and/or move up to 25 pounds. The noise level in the work environment is usually moderately quiet, with frequent interruptions and multiple demands.
Additional Information
OUR CULTURAL BELIEFS:
Patient Minded I act with the patient’s best interest in mind.
Client Delight I own every client experience and its impact on results.
Take Action I am empowered and empower others to act now.
Grow Talent I own my development and invest in the development of others.
Win Together I passionately connect with anyone, anywhere, anytime to achieve results.
Communication Matters I speak up to create transparent, thoughtful and timely dialogue.
Embrace Diversity I create an environment of awareness and respect.
Always Innovate I am bold and creative in everything I do.
Our team is aware of recent fraudulent job offers in the market, misrepresenting EVERSANA. Recruitment fraud is a sophisticated scam commonly perpetrated through online services using fake websites, unsolicited e-mails, or even text messages claiming to be a legitimate company. Some of these scams request personal information and even payment for training or job application fees. Please know EVERSANA would never require personal information nor payment of any kind during the employment process. We respect the personal rights of all candidates looking to explore careers at EVERSANA.
EVERSANA is committed to providing competitive salaries and benefits for all employees. If this job posting includes a base salary range, it represents the low and high end of the salary range for this position and is not applicable to locations outside of the U.S. Compensation will be determined based on relevant experience, other job-related qualifications/skills, and geographic location (to account for comparative cost of living). More information about EVERSANA’s benefits package can be found at eversana.com/careers. EVERSANA reserves the right to modify this base salary range and benefits at any time.
From EVERSANA’s inception, Diversity, Equity & Inclusion have always been key to our success. We are an Equal Opportunity Employer, and our employees are people with different strengths, experiences, and backgrounds who share a passion for improving the lives of patients and leading innovation within the healthcare industry. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one’s identity. All of our employees’ points of view are key to our success, and inclusion is everyone's responsibility.
Consistent with the Americans with Disabilities Act (ADA) and applicable state and local laws, it is the policy of EVERSANA to provide reasonable accommodation when requested by a qualified applicant or candidate with a disability, unless such accommodation would cause an undue hardship for EVERSANA. The policy regarding requests for reasonable accommodations applies to all aspects of the hiring process. If reasonable accommodation is needed to participate in the interview and hiring process, please contact us at applicantsupport@eversana.com.
Company Description
At EVERSANA®, we are proud to be a Great Place to Work across the globe. We’re fueled by our vision to create a healthier world. How? Our global team of more than 6,000 employees is committed to creating and delivering next-generation commercialization services to the life sciences industry. We are grounded in our cultural beliefs and serve more than 670 clients ranging from innovative biotech start-ups to established pharmaceutical companies. Our products, services and solutions help bring innovative therapies to market and support the patients who depend on them. Our jobs, skills and talents are unique, but together we make an impact every day. Join us!
Across our growing organization, we embrace diversity in backgrounds and experiences. Improving patient lives around the world is a priority, and we need people from all backgrounds and swaths of life to help build the future of the healthcare and the life sciences industry. We believe our people make all the difference in cultivating an inclusive culture that embraces our cultural beliefs. We are deliberate and self-reflective about the kind of team and culture we are building. We look for team members that are not only strong in their own aptitudes but also who care deeply about EVERSANA, our people, clients and most importantly, the patients we serve. We are EVERSANA.
Job Description
THE POSITION:
The Medical, Legal and Regulatory (MLR) review is an essential process in healthcare marketing to make sure advertising, promotional and non-promotional content is accurate, compliant, and ready to be published. The MLR process must rigorously control and execute review, approval and document filing actions. As part of the MLR team, the Medical, Legal and Regulatory (MLR) Coordinator is responsible for managing all the MLR processes for a dedicated client. The Medical, Legal and Regulatory (MLR) Coordinator ensures that all administrative and program management support for the client’s MLR process operates effectively and in full compliance with all internal and external policies and regulations.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Our employees are tasked with delivering excellent business results through the efforts of their teams. These results are achieved by:
MEDICAL, LEGAL AND REGULATORY (MLR) COORDINATOR RESPONSIBILITIES
- Manages the end-to-end MLR process.
- Responsible for scheduling, setting the agenda, and leading Review Committee meetings.
- Add live discussion notes for comments discussed in Veeva Vault.
- Scribe meeting minutes, circulate draft meeting minutes for Committee approval and finalize and file approved minutes.
- Ensure all covered communications are properly vetted through the review process utilizing the online review system (e.g., Veeva Vault PromoMats and Vault MedComms).
- Cascade and enforce any new policies and guidelines related to review of materials.
- Verifies that materials are assigned to the appropriate review path. Rejects incomplete submissions and materials that are not review ready. Facilitates/documents discussion in live meetings.
- QCs Final Document vs. Approved Document.
- Supports FDA 2253 submissions, or country specific regulatory submissions with MLR Regulatory Reviewer/Partner.
MEDICAL CONTENT SUPPORT RESPONSIBILITIES
- Support the development of project plans.
- Support medical content development team.
- Support upload of materials into clients’ review and approval platforms, including supporting annotating, anchoring references, etc.
MEDICAL AFFAIRS AND MEDICAL INFORMATION PROJECT MANAGEMENT SUPPORT
- Support Medical Affairs and Medical Information leadership in developing and managing project plans for key initiatives.
- Demonstrate a commitment to diversity, equity, and inclusion through continuous development, modeling inclusive behaviors, and proactively managing bias.
- All other duties as assigned.
Consistent with the Americans with Disabilities Act (ADA) and applicable state and local laws, it is the policy of EVERSANA to provide reasonable accommodation when requested by an employee with a disability, unless such accommodation would cause an undue hardship for EVERSANA. If reasonable accommodation is needed to perform the essential functions of your job position, please contact Human Resources.
EXPECTATIONS OF THE JOB:
- Travel: In general, this position does not travel.
- Hours: Able to work full-time and be flexible with work scheduling as required by clients and management.
- Metrics: Maintain and contribute toward process improvement which positively impacts metrics associated with activities of the MLR Review process; metrics are subject to change annually or more often as deemed necessary.
- Customer Services: Maintain and improve customer services associated with the activity of the MLR review.
- Time Management: Complete MLR coordination responsibilities in a timely manner.
The above list reflects the general details necessary to describe the expectations of the position and shall not be construed as the only expectations that may be assigned for the position.
An individual in this position must be able to successfully perform the expectations listed above.
Qualifications
MINIMUM KNOWLEDGE, SKILLS AND ABILITIES:
The requirements listed below are representative of the experience, education, knowledge, skill and/or abilities required.
- Education: Graduates in any Life Sciences / Biomedical field.
- Must demonstrate excellent ability to communicate effectively in English, both orally and in writing.
- Experience and/or Training:
- At least 2 years of experience in a healthcare agency or pharmaceutical company.
- Experience with use of Veeva Vault PromoMats / MedComms.
- Experience in Scientific Writing / Scientific Reviewing / MLR.
- Project management.
- Time management.
- Meeting management.
- Excellent customer service skills.
- Technology/Equipment: Computer proficiency in Outlook and Microsoft Office Suite (Word, Excel, PowerPoint, and other Window applications).
PREFERRED QUALIFICATIONS:
- Education: Graduates/Postgraduates in Pharmacy or Medicine preferred.
- Experience and/or Training
- Working knowledge of or familiarity with global healthcare compliance statutes and laws.
- Ability to perform assignments with a high degree of independence requiring extensive experience, skill, and knowledge.
- Excellent computer skills including competency in presentation, word processing and spreadsheet software, utilizing MS Office Suite.
- Proven ability to manage multiple tasks, set priorities and meet deadlines.
- Ability to manage cross-functional projects.
- Familiar with laws and regulations regarding US drug/device advertising and promotion, including industry best practices.
- Knowledge of medical terminology (preferred but not required).
- Must be quality-oriented and demonstrate consistent attention to detail.
- Must have the ability to follow established processes and procedures and the flexibility to adopt new practices and priorities as required.
- Positive Attitude and Energy – Exhibits an upbeat attitude, a genuine interest in others and a sense of humor. Energizes others and heightens morale through her/his attitude.
- Communication Skills – Possesses the ability to develop and articulate ideas and information that generate understanding and create a climate that motivates and encourages others to participate.
- Innovator – Transforms creative ideas into original solutions that positively impact the company’s performance.
- Highly Principled – Proves to be a professional of unquestionable integrity, credibility and character who demonstrates high moral and ethical behavior.
PHYSICAL/MENTAL DEMANDS AND WORKING ENVIRONMENT:
The physical and mental requirements along with the work environment characteristics described here are representative of those an individual encounters while performing the essential functions of this position.
Office: While performing the essential functions of this job the employee is frequently required to reach, grasp, stand and/or sit for long periods of time (up to 90% of the shift), walk, talk and hear; occasionally required to lift and/or move up to 25 pounds. The noise level in the work environment is usually moderately quiet, with frequent interruptions and multiple demands.
Additional Information
OUR CULTURAL BELIEFS:
Patient Minded I act with the patient’s best interest in mind.
Client Delight I own every client experience and its impact on results.
Take Action I am empowered and empower others to act now.
Grow Talent I own my development and invest in the development of others.
Win Together I passionately connect with anyone, anywhere, anytime to achieve results.
Communication Matters I speak up to create transparent, thoughtful and timely dialogue.
Embrace Diversity I create an environment of awareness and respect.
Always Innovate I am bold and creative in everything I do.
Our team is aware of recent fraudulent job offers in the market, misrepresenting EVERSANA. Recruitment fraud is a sophisticated scam commonly perpetrated through online services using fake websites, unsolicited e-mails, or even text messages claiming to be a legitimate company. Some of these scams request personal information and even payment for training or job application fees. Please know EVERSANA would never require personal information nor payment of any kind during the employment process. We respect the personal rights of all candidates looking to explore careers at EVERSANA.
EVERSANA is committed to providing competitive salaries and benefits for all employees. If this job posting includes a base salary range, it represents the low and high end of the salary range for this position and is not applicable to locations outside of the U.S. Compensation will be determined based on relevant experience, other job-related qualifications/skills, and geographic location (to account for comparative cost of living). More information about EVERSANA’s benefits package can be found at eversana.com/careers. EVERSANA reserves the right to modify this base salary range and benefits at any time.
From EVERSANA’s inception, Diversity, Equity & Inclusion have always been key to our success. We are an Equal Opportunity Employer, and our employees are people with different strengths, experiences, and backgrounds who share a passion for improving the lives of patients and leading innovation within the healthcare industry. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one’s identity. All of our employees’ points of view are key to our success, and inclusion is everyone's responsibility.
Consistent with the Americans with Disabilities Act (ADA) and applicable state and local laws, it is the policy of EVERSANA to provide reasonable accommodation when requested by a qualified applicant or candidate with a disability, unless such accommodation would cause an undue hardship for EVERSANA. The policy regarding requests for reasonable accommodations applies to all aspects of the hiring process. If reasonable accommodation is needed to participate in the interview and hiring process, please contact us at applicantsupport@eversana.com.
Medical Coordinator Job Roles in Kansas
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Search Medical Coordinator Jobs in KansasMedical Coordinator Jobs in Kansas: Frequently Asked Questions
Which companies sponsor visas for medical coordinators in Kansas?
The University of Kansas Health System in Kansas City, Ascension Via Christi across Wichita and surrounding communities, and Stormont Vance Regional Health in Topeka are among the larger Kansas employers with documented visa sponsorship history for healthcare coordination roles. Regional health networks and federally qualified health centers sometimes sponsor too, particularly for roles tied to Medicaid care management or chronic disease coordination programs.
Which visa types realistically fit medical coordinator roles in Kansas?
Medical coordinator roles typically qualify for H-1B visa sponsorship when the position requires a bachelor's degree in a directly related field such as health administration, nursing, or public health. EB-2 and EB-3 employment-based green cards are also relevant for permanent sponsorship through PERM labor certification. F-1 OPT and STEM OPT can apply for recent graduates whose degree is in a qualifying field. J-1 visa exchange visitor status may be available through designated sponsor organizations.
Which cities in Kansas have the most medical coordinator sponsorship jobs?
Wichita has the highest concentration of medical coordinator openings in Kansas, driven by Ascension Via Christi, Wesley Medical Center, and a cluster of specialty clinics. Kansas City, Kansas is the second major hub, anchored by The University of Kansas Health System and its network of outpatient facilities. Topeka and Lawrence also post medical coordinator roles regularly, particularly tied to state health programs and university-affiliated clinics.
How to find medical coordinator visa sponsorship jobs in Kansas?
Migrate Mate lists Kansas medical coordinator roles specifically filtered to employers with verified visa sponsorship history, so you can focus your search on positions where sponsorship is a documented practice rather than an open question. Searching by city within Migrate Mate lets you narrow results to Wichita, Kansas City, or Topeka based on where you want to work, and role-specific filters help distinguish coordinator positions from broader administrative or clinical titles.
Are there state-specific factors that affect medical coordinator visa sponsorship in Kansas?
Kansas has a significant rural health shortage, and several employers in underserved counties qualify for special federal programs that can support hiring and retention of international healthcare staff. The University of Kansas School of Medicine also generates a local pipeline of graduates who transition into coordination roles, meaning employers in the state are generally familiar with credential evaluation and sponsorship processes for healthcare administration candidates. Cap-exempt institutions like academic medical centers may offer more consistent H-1B sponsorship outside the annual lottery.
What is the prevailing wage for sponsored medical coordinator jobs in Kansas?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.