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Medical Director Clinical Development Jobs in Kansas

ICON Clinical Research

Medical Monitor

Lenexa, KS · On-site

As a Medical Director, Clinical Research & Development at ICON, you will provide medical leadership and strategic direction to clinical development programs. We are looking for a board certified ...

Wellpath

Medical Director

Kansas City, KS · On-site

... clinical care, which includes lives saved by Narcan. We offer ongoing training and development ... How you make a difference The Site Medical Director provides clinical leadership at the assigned ...

Wellpath

Medical Director

Kansas City, KS · On-site

$66K - $73K/yr

... clinical care, which includes lives saved by Narcan. We offer ongoing training and development ... How you make a difference The Site Medical Director provides clinical leadership at the assigned ...

Wellpath

Medical Director

Kansas City, KS · On-site

... clinical care, which includes lives saved by Narcan. We offer ongoing training and development ... How you make a difference The Site Medical Director provides clinical leadership at the assigned ...

Wellpath

Medical Director

Kansas City, KS · On-site

... clinical care, which includes lives saved by Narcan. We offer ongoing training and development ... The Site Medical Director provides clinical leadership at the assigned facility and ensures ...

Hunter Health

Medical Director

Wichita, KS · On-site

Medical Director Opportunity This is more than a physician role--it is an opportunity to help shape ... This role also provides clinical leadership, mentorship, and provider development for physicians ...

Hunter Health

Medical Director

Wichita, KS · On-site

Medical Director Opportunity This is more than a physician role-it is an opportunity to help shape ... This role also provides clinical leadership, mentorship, and provider development for physicians ...

Hunter Health

Medical Director

Wichita, KS · On-site

Medical Director Opportunity This is more than a physician role-it is an opportunity to help shape ... This role also provides clinical leadership, mentorship, and provider development for physicians ...

Wellpath

Medical Director

Kansas City, KS · On-site

... development. They also play a key role in chronic care clinic oversight, pharmacy monitoring, and medical program review. Responsibilities * Provide direct medical care and document all clinical ...

Trinity Health

Medical Director

Saint Francis, KS

This role provides leadership in medical policy development, supervises Primary Care Providers ... Provide clinical leadership in team meetings and support the care of frail or elderly participants.

Trinityhealth

Medical Director

Saint Francis, KS

This role provides leadership in medical policy development, supervises Primary Care Providers ... Provide clinical leadership in team meetings and support the care of frail or elderly participants.

CareArc Inc

Medical Director

Emporia, KS · On-site

The Medical Director collaborates closely with administrative leadership to advance the ... Oversee the development and implementation of clinical policies, workflows, and protocols.

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All JobsMedical Clinical Development JobsMedical Director Clinical Development JobsMedical Director Clinical Development Jobs in Kansas

Medical Director Clinical Development information

See Kansas salary details

$11.6K

$207.2K

$318.4K

How much do medical director clinical development jobs pay per year?

As of Aug 27, 2026, the average yearly pay for medical director clinical development in Kansas is $207,238.00, according to ZipRecruiter salary data. Most workers in this role earn between $176,600.00 and $253,700.00 per year, depending on experience, location, and employer.

What does a medical director clinical development do?

A Medical Director of Clinical Development is responsible for overseeing the planning, execution, and management of clinical trials for new drugs or medical products. They work closely with cross-functional teams, such as regulatory affairs, clinical operations, and research scientists, to ensure that clinical studies are designed effectively and conducted in compliance with regulatory standards. Their role also includes reviewing and interpreting clinical data, providing medical expertise, and contributing to the overall strategy for product development. Medical Directors play a crucial role in ensuring the safety and efficacy of new therapies before they reach the market.

How does a medical director clinical development typically collaborate with cross-functional teams during a clinical trial?

As a Medical Director in Clinical Development, you will regularly collaborate with cross-functional teams such as clinical operations, regulatory affairs, biostatistics, data management, and pharmacovigilance. Your role involves providing medical and scientific guidance, ensuring protocol adherence, and addressing safety or efficacy concerns throughout the trial. Effective communication and teamwork are essential for aligning on trial objectives, managing timelines, and resolving any emerging issues. This collaborative environment fosters a comprehensive approach to advancing clinical programs and supports the successful execution of clinical trials.

What are the key skills and qualifications needed to thrive as a medical director clinical development, and why are they important?

To thrive as a Medical Director Clinical Development, you need an advanced medical degree (MD or equivalent), extensive clinical research experience, and a deep understanding of regulatory requirements and drug development processes. Familiarity with electronic data capture systems, clinical trial management software, and GCP/ICH guidelines is typically required. Strong leadership, strategic thinking, and exceptional communication skills help drive multidisciplinary teams and manage complex projects. These skills ensure the safe, efficient, and compliant progression of clinical programs from conception through regulatory approval.

What is the difference between Medical Director Clinical Development vs Medical Scientist?

AspectMedical Director Clinical DevelopmentMedical Scientist
Required CredentialsMD or DO, clinical research experience, industry certificationsMD, PhD, or equivalent, research-focused
Work EnvironmentPharmaceutical companies, biotech firms, clinical trial oversightResearch institutions, academia, laboratories
Employer & Industry UsageCommonly employed in industry to oversee clinical developmentPrimarily in research and academia, less in industry

The Medical Director Clinical Development typically oversees clinical trials and ensures regulatory compliance within the industry, requiring medical credentials and industry experience. Medical Scientists focus on research and discovery, often working in labs or academic settings. While both roles require advanced degrees, their work environments and primary responsibilities differ significantly.

What are popular job titles related to Medical Director Clinical Development jobs in Kansas?

For Medical Director Clinical Development jobs in Kansas, the most frequently searched job titles are:

What job categories do people searching Medical Director Clinical Development jobs in Kansas look for?

The top searched job categories for Medical Director Clinical Development jobs in Kansas are:

What cities in Kansas are hiring for Medical Director Clinical Development jobs?

Cities in Kansas with the most Medical Director Clinical Development job openings:

Medical Director Clinical Development jobs near you

Medical Monitor

Lenexa, KS • On-site

ICON Clinical Research
Biotechnology Research and Development • 201 - 500 employees
Learn more about ICON Clinical Researchexternal

Other

Medical, Life, Retirement, PTO

Posted 19 days ago

Job description

Medical Monitor

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

As a Medical Director, Clinical Research & Development at ICON, you will provide medical leadership and strategic direction to clinical development programs. We are looking for a board certified professional with experience in monitoring Obesity/GLP-1 studies.

What You Will Do:

You will lead medical affairs delivery across your portfolio, setting standards and developing your team.

Key responsibilities include:

  • Providing medical and scientific oversight for clinical trials, ensuring that study protocols are scientifically sound and aligned with regulatory requirements.

  • Collaborating with clinical operations, regulatory, and safety teams to drive the successful execution of clinical development programs.

  • Developing and reviewing clinical study protocols, investigator brochures, and other key study documents.

  • Interpreting clinical trial data and providing medical insights to inform decision-making and guide clinical development strategies.

  • Building relationships with key opinion leaders, investigators, and external stakeholders to support clinical development initiatives.

Your Profile:

You will bring significant medical affairs experience, with a track record of building high-performing teams and delivering results.

Required qualifications and experience:

  • Medical degree (MD) or equivalent qualification.

  • Extensive experience in clinical research and development, preferably within the pharmaceutical or biotechnology industry.

  • Strong understanding of clinical trial design, regulatory requirements, and GCP guidelines.

  • Exceptional analytical and problem-solving skills, with a focus on interpreting clinical data and driving evidence-based decisions.

  • Excellent leadership, communication, and collaboration skills, with the ability to work effectively in cross-functional, global teams.

  • Willingness to travel as required (approximately 10%)

What ICON can offer you:

Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements

  • A range of health insurance offerings to suit you and your family's needs.

  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.

  • Life assurance

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

Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (https://careers.iconplc.com/reasonable-accommodations)

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply

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