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Clinical Trial Risk Based Monitoring Jobs in Kansas

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 ...

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 ...

ICON plc

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 ...

410 ICR United States USA

Clinical Dietary Aide

Lenexa, KS

$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 ...

Icon plc

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 ...

410 ICR United States USA

Clinical Dietary Aide

Lenexa, KS

$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 ...

micro1 AI

Hematologist / Oncologist

Overland Park, KS · Remote

$160 - $200/hr

Evaluate benefit-risk reasoning, scrutinizing the durability of conclusions in light of new events ... Peer-reviewed publication record or authorship on clinical trial manuscripts, with any exposure to ...

micro1 AI

Hematologist / Oncologist

Kansas City, KS · Remote

$160 - $200/hr

Evaluate benefit-risk reasoning, scrutinizing the durability of conclusions in light of new events ... Peer-reviewed publication record or authorship on clinical trial manuscripts, with any exposure to ...

micro1 AI

Hematologist / Oncologist

Topeka, KS · Remote

$160 - $200/hr

Evaluate benefit-risk reasoning, scrutinizing the durability of conclusions in light of new events ... Peer-reviewed publication record or authorship on clinical trial manuscripts, with any exposure to ...

micro1 AI

Hematologist / Oncologist

Olathe, KS · Remote

$160 - $200/hr

Evaluate benefit-risk reasoning, scrutinizing the durability of conclusions in light of new events ... Peer-reviewed publication record or authorship on clinical trial manuscripts, with any exposure to ...

micro1 AI

Hematologist / Oncologist

Wichita, KS · Remote

$160 - $200/hr

Evaluate benefit-risk reasoning, scrutinizing the durability of conclusions in light of new events ... Peer-reviewed publication record or authorship on clinical trial manuscripts, with any exposure to ...

Parexel

Leads day to day project activities in the matrix, by working closely with the Clinical Trial ... Evaluate performance and solve acute challenges and monitor timelines and progress vs. plan

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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.

How to become a clinical trial risk based monitoring?

To become a clinical trial risk-based monitor, candidates typically need a bachelor's degree in life sciences, healthcare, or related fields, along with experience in clinical research or monitoring. Certification such as the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA) can enhance job prospects. Strong knowledge of Good Clinical Practice (GCP) guidelines and proficiency with electronic data capture (EDC) systems are also important.

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:
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Clinical Trial Risk Based Monitoring jobs near you

Manager of Clinical Operations

Argenta

Shawnee, KS • On-site

Full-time

Re-posted 2 days ago

Job description

At Argenta, we partner with our customers to take animal health solutions from molecule to market. Our teams combine deep scientific expertise with world-class manufacturing capabilities to deliver innovative therapies that improve the lives of animals around the world.
About the Role
Argenta is seeking a Manager of Clinical Operations to join our US Clinical team. This role will work closely with the Head of US Clinical on leading the execution of the US Clinical strategy and business plan while building and maintaining a high performance culture.
You will help to manage client expectations while collaborating, mentoring and supporting US Clinical staff to ensure deliverables are met and accountability maximized.
This is an exciting opportunity for a technically sound operational leader who thrives in high performing environments with a hybrid workforce.
Key Responsibilities
  • Leads the execution of the Clinical strategy and business plan
  • Builds and maintains a high-performance culture through championing effective performance, processes, communication, and coaching and development of staff
  • Provides timely, relevant, and accurate reporting to the Head of US Clinical &/or Executive team
  • Effectively manages client and other stakeholder expectations through relevant communication
  • Coordinate and assign tasks to clinical personnel and ensure projects are compliant with Good Clinical Practice Guidelines (if applicable) to deliver high quality data to the study Sponsors
  • Implement, and maintain strategies and training for CTM, CRA, and Clinical Support teams
  • Recommends, develops, and regularly facilitates innovative learning for Clinical Research Associates of all levels. Training should be evaluated regularly and updated as the needs of the business unit change. Facilitation is co-facilitated among the CRA Team Leads

About You
  • Bachelor's degree in science related field, advanced degree preferred.
  • 5+ years' experience in clinical trial management or clinical operations management
  • A collaborative working style to be able to lead and motivate people at all levels and across all functions in an organization
  • Strong analytical thinking and problem-solving skills
  • Capable of working in a changing environment and under pressure
  • Develops new insights into situations and applies creative and fresh solutions to make improvements
  • Ability to identify new ideas, methodologies, different positions, and alternatives to improve clinical monitoring services of Clinical R&D
  • Supports organizational goals and objectives aligned to strategic and/ or operations plans
  • Gathers key information essential to the planning and process of clinical trial management
  • Works collaboratively with key stakeholders to streamline operations for maximum efficiency, automation, and effectiveness where appropriate

Why Join Argenta?
At Argenta, we are building a culture of ownership where our people play a direct role in shaping the future of the organization. You will work alongside passionate experts across science, manufacturing and commercial functions to deliver life-changing outcomes for animals worldwide.
We offer the opportunity to work within a growing, global business where your leadership and expertise will have a meaningful impact on performance, transformation, and long-term success.
We are One Argenta - working together across teams, disciplines and geographies to create meaningful impact.

Apply