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Clinical Study Jobs in Kansas (NOW HIRING)

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Senior Study Manager - Infectious Disease/Vaccines (Pragmatic Trials) - US/Canada ICON is a global ... Establishes, leads and manages Clinical Trial Team (CTT) Supports clinical (drug/vaccine) supplies ...

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In this role, you will lead global clinical trials from sourcing strategy and RFP development through study start-up, execution, database release, and inspection readiness-ensuring the timely ...

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Study Start Up Associate II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...

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Study Start Up Associate II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...

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Leading the preparation, review, and editing of clinical study documents, including clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and regulatory submissions ...

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Clinical Study information

See Kansas salary details

$19.6K

$111.7K

$183.7K

How much do clinical study jobs pay per year?

As of Aug 5, 2026, the average yearly pay for clinical study in Kansas is $111,740.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,800.00 and $140,000.00 per year, depending on experience, location, and employer.

What is a clinical study?

Clinical studies are research investigations conducted with human volunteers to evaluate the safety, effectiveness, and side effects of medical treatments, drugs, devices, or interventions. These studies follow strict scientific and ethical guidelines and are usually carried out in several phases before a treatment can be approved for widespread use. Clinical studies help determine whether new approaches to prevention, diagnosis, or therapy are safe and effective for people. Participation in clinical studies is voluntary and can contribute to advancements in medical science.

What are some common challenges faced when managing multiple clinical studies simultaneously?

Professionals involved in clinical studies often juggle several projects at once, which can present challenges such as balancing competing timelines, ensuring regulatory compliance across studies, and coordinating with diverse teams. Effective project management, clear communication, and strong organizational skills are key to addressing these challenges. Utilizing project management tools and maintaining detailed documentation can help keep studies on track and reduce the risk of errors or delays.

Do clinical studies pay well?

Clinical study roles, such as clinical research coordinators or assistants, typically offer moderate pay that varies by experience, location, and employer. Entry-level positions may start at lower wages, while experienced professionals or those with specialized skills can earn higher salaries, especially when working on complex or long-term studies.

What is the difference between Clinical Study vs Clinical Research Coordinator?

AspectClinical StudyClinical Research Coordinator
CredentialsOften requires a degree in health sciences, nursing, or related fields; certifications like CCRP are commonTypically holds a bachelor's degree in health sciences, nursing, or related fields; certifications like CCRP or CRC are advantageous
Work EnvironmentConducted in hospitals, clinics, or research facilities; involves direct patient interaction and data collectionWorks in research sites, hospitals, or clinics; manages study logistics and coordinates between teams
Employer & IndustryPharmaceutical companies, academic institutions, CROsResearch institutions, hospitals, pharmaceutical companies

While both roles are integral to clinical research, a Clinical Study typically refers to the overall research process or specific studies, whereas a Clinical Research Coordinator is a professional who manages and oversees the day-to-day operations of clinical trials. Understanding these distinctions helps in choosing the right career path or job search focus.

What jobs are there in clinical studies?

Jobs in clinical studies include clinical research coordinators, clinical research associates, data managers, regulatory affairs specialists, and study nurses. These roles involve tasks such as patient recruitment, data collection, monitoring trial progress, and ensuring compliance with regulations, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications. The work environment is typically a research facility, hospital, or pharmaceutical company, with schedules varying from full-time to part-time depending on the role.

What are the key skills and qualifications needed to thrive as a clinical study coordinator?

To thrive as a Clinical Study Coordinator, you need a solid understanding of clinical research protocols, regulatory guidelines like GCP, and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certification such as CCRC or CCRA is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating multiple tasks and interacting with diverse stakeholders. These skills ensure compliance, accurate data collection, and smooth trial operations, which are vital for the integrity and success of clinical studies.
What are the most commonly searched types of Clinical Study jobs in Kansas? The most popular types of Clinical Study jobs in Kansas are:
What cities in Kansas are hiring for Clinical Study jobs? Cities in Kansas with the most Clinical Study job openings:
Clinical Study jobs near you
Infographic showing various Clinical Study job openings in Kansas as of July 2026, with employment types broken down into 2% As Needed, 74% Full Time, 16% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $111,740 per year, or $53.7 per hour.

Senior Study Manager - Infectious Disease/Vaccines (Pragmatic trials) - US/Canada

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Full-time

Medical, Dental, Vision, Life, Retirement

Posted 28 days ago

Job description

Senior Study Manager - Infectious Disease/Vaccines (Pragmatic Trials) - US/Canada

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


Senior Study Manager

May lead or support a study or studies, depending on size/complexity. As lead, will be responsible for the following:

  • Operational point of contact for trial execution and all trial deliverables

  • Manages all HQ Operational Activities, including: Establishes, leads and manages Clinical Trial Team (CTT) Supports clinical (drug/vaccine) supplies planning

  • Manages deployment and interactions with external vendors (e.g., IVRS, PRO)

  • Initiates planning for Investigator meeting and protocol training.

  • Plans and assesses protocol ancillary supplies

  • Completes trial set-up and maintains CTMS

  • Schedules, prepares for, and leads the Recruitment Planning Meeting for the CTT

  • Initiates recruitment/retention planning & enrollment tracking Responsible for tracking study related details (e.g., specimens, queries)

  • Oversees protocol training activities including IMs and CRAs training meetings

  • Ensures appropriate postings to investigative site portals

  • Responsible for operational deliverables in preparation for site ready, country allocation and achievement of recruitment targets (with input from others)

  • Point of escalation for study related operational issues

  • Responsible for operational details at Operational Reviews

  • Responsible for creating and maintaining project schedule and collaborating with Program Lead

  • Sets up and maintains Trial Master File (eTMF)

  • Ensures alignment of budget with protocol needs

  • Responsible for executing protocol within the budget

  • Responsible for creating and maintaining ADI logs

  • Develops Site Monitoring Plan (SMP) with input from the monitoring excellence group

  • Develops study related manuals (e.g., administrative binder, lab manuals)

  • Manages Emergency Unblinding (EUB) Call Center activities

  • Co-authors newsletters with CS

  • Approves contracts, invoice payments and change orders for vendors, as necessary

  • Responsible for end of study reconciliation (clinical & ancillary supplies)

  • Oversees all HQ close-out tasks

  • Responsible for ongoing monitoring of trial activities, e.g. dashboards, tracking

  • Supports CS activities as needed to achieve CTT deliverables

  • Interface with External Data Coordination and Data Management

  • Responsible for quality control and inspection readiness at all times

  • Responsible for risk assessment, mitigation planning and execution

What you need to have:

  • BS/BA/MS/PhD with 7+ yrs clinical research experience Minimum Years of Experience

  • Minimum 2 years pharmaceutical experience with demonstrated leadership responsibilities required.

  • Proven ability to meet aggressive timelines

  • MS Project experience preferred

  • Excellent Excel and PP skills required

  • TA- Infectious disease and/or vaccines experience highly preferred

  • Global experience required

  • Excellent oral (including presentation) and written communication, computer/database management, and project management skills required

  • Home Based position in US or Canada

Areas of direct experience:

  • Protocol design for pragmatic trials

  • Site/site network selection

  • Integration with healthcare systems

  • Informed consent approaches (simplified, eConsent, etc.)

  • Use of EHR / real-world data

  • Endpoint definition (e.g., hospitalization, utilization)

  • Central vs site monitoring approaches

  • Vendor/technology integration

  • Regulatory interactions / submissions


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Are you a current ICON Employee? Please click here to apply

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