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Clinical Trial Risk Based Monitoring Jobs in Kansas

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Clinical Dietary Aide

Lenexa, KS · On-site

$12.75 - $16/hr

Delivering meals and snacks to clinical trial participants according to dietary requirements and study schedules. * Ensuring accurate labeling, portioning, and timing of meals based on protocol ...

Argenta

Manager of Clinical Operations

Shawnee, KS · Hybrid

... monitoring services of Clinical R&D * Supports organizational goals and objectives aligned to ... Gathers key information essential to the planning and process of clinical trial management * Works ...

Argenta

Manager of Clinical Operations

Shawnee, KS · On-site

... monitoring services of Clinical R&D * Supports organizational goals and objectives aligned to ... Gathers key information essential to the planning and process of clinical trial management * Works ...

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Establishes, leads and manages Clinical Trial Team (CTT) Supports clinical (drug/vaccine) supplies ... Develops Site Monitoring Plan (SMP) with input from the monitoring excellence group * Develops ...

ICON

Clinical Dietary Aide

Lenexa, KS · On-site

$12.75 - $16/hr

Delivering meals and snacks to clinical trial participants according to dietary requirements and study schedules. * Ensuring accurate labeling, portioning, and timing of meals based on protocol ...

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$65K - $86K/yr

Analyzing and developing pricing strategies for clinical trial investigators, ensuring alignment ... based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package ...

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Understanding of clinical trial operations with specific knowledge of informed consent forms ... risk language * Work with protocol authors to ensure comprehensive understanding of protocol ...

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Trial Delivery Leader ICON is a global healthcare intelligence and clinical research organisation ... Developing and managing program plans, timelines, budgets, and resources, monitoring progress and ...

IQVIA

Sr. Clinical Research Associate, IQVIA

Lenexa, KS

$101K - $169K/yr

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and ... Ensure copies/originals (as required) site documents are available for filing in the Trial Master ...

IQVIA

Sr. Clinical Research Associate, IQVIA

Lenexa, KS · On-site

$101K - $169K/yr

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and ... Ensure copies/originals (as required) site documents are available for filing in the Trial Master ...

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Clinical Trial Risk Based Monitoring information

How does a Clinical Trial Risk Based Monitoring professional typically collaborate with cross-functional teams during a study?

In a Clinical Trial Risk Based Monitoring role, you will regularly work with clinical research associates, data managers, statisticians, and regulatory teams to identify and address potential risks throughout a study. Collaboration often involves participating in meetings to review data trends, sharing insights about site performance, and helping to develop mitigation strategies. Effective communication is crucial, as you will be responsible for ensuring that all stakeholders are informed of key risks and recommended actions. This collaborative environment helps drive patient safety, data integrity, and overall trial success.

What is the difference between Clinical Trial Risk Based Monitoring vs Clinical Trial Data Manager?

AspectClinical Trial Risk Based MonitoringClinical Trial Data Manager
Primary FocusMonitoring trial sites for risks and complianceManaging and ensuring accuracy of trial data
Required SkillsMonitoring protocols, regulatory knowledge, site managementData management, database systems, quality control
Work EnvironmentClinical sites, monitoring visits, remote oversightData centers, clinical trial databases, office setting
CertificationsGCP, monitoring certificationsCDMP, data management certifications

While both roles are integral to clinical trials, Risk Based Monitoring focuses on overseeing site performance and compliance to mitigate risks, whereas Data Managers concentrate on managing and validating trial data for accuracy and integrity.

What is Clinical Trial Risk Based Monitoring?

Clinical Trial Risk Based Monitoring (RBM) is a strategy used in clinical research to prioritize and focus monitoring activities on the most critical risks to patient safety and data integrity. Instead of monitoring every data point equally, RBM uses data analytics and risk assessment tools to identify which sites, processes, or data require more attention. This approach increases efficiency, reduces costs, and helps ensure that potential issues are detected and addressed promptly. RBM is supported by regulatory agencies and is increasingly adopted in both large and small clinical trials.

What are the key skills and qualifications needed to thrive in Clinical Trial Risk Based Monitoring, and why are they important?

To thrive in Clinical Trial Risk Based Monitoring, you need expertise in clinical research, regulatory compliance, and data analysis, usually supported by a degree in life sciences or related fields. Familiarity with risk assessment tools, EDC (Electronic Data Capture) systems, and GCP (Good Clinical Practice) certification is typically required. Strong attention to detail, critical thinking, and effective communication help professionals proactively identify and address potential risks in trials. These skills are crucial for maintaining data integrity, ensuring patient safety, and optimizing the efficiency and quality of clinical studies.
What are popular job titles related to Clinical Trial Risk Based Monitoring jobs in Kansas? For Clinical Trial Risk Based Monitoring jobs in Kansas, the most frequently searched job titles are:
What job categories do people searching Clinical Trial Risk Based Monitoring jobs in Kansas look for? The top searched job categories for Clinical Trial Risk Based Monitoring jobs in Kansas are:
What cities in Kansas are hiring for Clinical Trial Risk Based Monitoring jobs? Cities in Kansas with the most Clinical Trial Risk Based Monitoring job openings:
Clinical Trial Risk Based Monitoring jobs near you
Clinical Dietary Aide

Clinical Dietary Aide

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Lenexa, KS • On-site

$12.75 - $16/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 9 days ago

Job description

Clinical Dietary Aide

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.


We are seeking a Clinical Dietary Aide to support meal service operations within our clinical research unit at ICON. In this role, you will help ensure that clinical trial participants receive meals and snacks safely, accurately, and on schedule. This includes preparing meal areas, delivering trays, maintaining kitchen and dining spaces, and providing friendly, patientfocused service throughout their stay.

This is an excellent role for candidates with experience as a dietary aide, food runner, server, cafeteria attendant, or hospitality associate who are interested in transitioning into a clinical research environment. The internal job title for this position is Medical Research Representative.

What You Will Be Doing

  • Preparing, stocking, and maintaining kitchen, cafeteria, and dining areas in accordance with safety, cleanliness, and foodhandling standards.

  • Setting up trays, utensils, beverages, and supplies needed for meal service.

  • Delivering meals and snacks to clinical trial participants according to dietary requirements and study schedules.

  • Ensuring accurate labeling, portioning, and timing of meals based on protocol guidelines.

  • Assisting with cleanup, including counters, equipment, dishes, carts, and dining areas.

  • Working with clinical staff to coordinate meal timing around study procedures or restrictions.

  • Providing excellent customer service to participants to ensure a comfortable and positive dining experience.

  • Reporting participant needs or concerns promptly to the clinical team.

  • Supporting general clinic operations with light administrative or participantsupport tasks as needed.

Your Profile

  • Experience in dietary aide, food service, hospitality, senior living, or customer service roles.

  • Strong attention to cleanliness, organization, and foodsafety procedures.

  • Excellent communication, teamwork, and customer service skills.

  • Ability to multitask and work efficiently in a fastpaced environment.

  • Professional, reliable, and comfortable interacting with clinical trial participants.

  • Willingness to support flexible scheduling needs based on study activities.

  • No previous clinical experience required - training provided.

Why Join ICON?

  • Be part of a missiondriven team supporting clinical trials that advance patient health.

  • Gain exposure to the clinical research field with opportunities to learn and grow.

  • Supportive team environment with training provided for all responsibilities.

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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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