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Veeva Promomats Jobs in Kansas (NOW HIRING)

Veeva Promomats information

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$16

$43

$75

How much do veeva promomats jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for veeva promomats in Kansas is $43.02, according to ZipRecruiter salary data. Most workers in this role earn between $19.95 and $70.89 per hour, depending on experience, location, and employer.

What is Veeva Promomats?

Veeva Promomats is a cloud-based content management system designed specifically for the life sciences industry. It streamlines the process of creating, reviewing, approving, and distributing promotional materials while ensuring compliance with industry regulations. Promomats helps teams collaborate efficiently, maintain version control, and manage digital assets throughout their lifecycle. It is widely used by pharmaceutical, biotechnology, and medical device companies to ensure marketing and promotional materials meet both internal and external compliance standards.

What are the key skills and qualifications needed to thrive as a Veeva Promomats specialist?

To excel as a Veeva Promomats Specialist, you need a solid understanding of content management, regulatory compliance, and familiarity with pharmaceutical or life sciences processes, often backed by a relevant degree. Expertise in using Veeva Vault Promomats, document management systems, and knowledge of FDA or EMA regulations is typically required, with Veeva certifications being advantageous. Strong attention to detail, communication, and problem-solving skills help facilitate collaboration between cross-functional teams and ensure accuracy. These capabilities are vital for maintaining compliance, streamlining workflows, and ensuring timely approval and distribution of promotional materials.

What are some common challenges faced by professionals working with Veeva Promomats, and how can they be addressed?

Professionals working with Veeva Promomats often encounter challenges such as adapting to evolving regulatory requirements, ensuring content accuracy, and managing efficient cross-functional collaboration. Navigating the platform’s workflows while maintaining compliance can be complex, especially when coordinating reviews between marketing, medical, and regulatory teams. To address these challenges, it's important to develop a strong understanding of Veeva’s features, proactively communicate with stakeholders, and stay updated on industry best practices for content management in the life sciences sector.

What is the difference between Veeva Promomats vs Veeva Vault?

AspectVeeva Promomats

Veeva Promomats is a cloud-based content management system specifically designed for managing promotional and medical content in the life sciences industry. Veeva Vault is a broader enterprise content management platform that supports various business processes, including quality, regulatory, and clinical data management. While Veeva Promomats focuses on promotional content workflows, Veeva Vault offers a comprehensive suite for multiple departments.

In summary, Veeva Promomats is specialized for promotional content management, making it ideal for marketing teams, whereas Veeva Vault provides a versatile platform for multiple enterprise functions across the life sciences sector.

What cities in Kansas are hiring for Veeva Promomats jobs?

Cities in Kansas with the most Veeva Promomats job openings:

Infographic showing various Veeva Promomats job openings in Kansas as of August 2026, with employment types broken down into 87% Full Time, 2% Part Time, and 11% Contract. Highlights an 72% Physical, 8% Hybrid, and 20% Remote job distribution, with an average salary of $89,483 per year, or $43 per hour.

Medical, Legal and Regulatory (MLR) Coordinator

EVERSANA

Overland Park, KS

Full-time

Re-posted 8 days ago


Eversana rating

6.7

Company rating: 6.7 out of 10

Based on 14 frontline employees who took The Breakroom Quiz

63rd of 72 rated business consultants


Job description

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.

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