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Clinical Trial Risk Based Monitoring Jobs in Louisiana

micro1 AI

Clinician (Oncology / Hematology)

New Orleans, LA · 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

Clinician (Oncology / Hematology)

Lafayette, LA · 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

Clinician (Oncology / Hematology)

Shreveport, LA · 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

Clinician (Oncology / Hematology)

Baton Rouge, LA · 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 ...

Ochsner Health

RN Clinical Research

New Orleans, LA

Provides patient care and assessment as determined necessary by the clinical trial in coordination ... Working knowledge in using computers, software, and web-based applications, including working ...

Ochsner Health

RN Clinical Research

New Orleans, LA · On-site

Provides patient care and assessment as determined necessary by the clinical trial in coordination ... Working knowledge in using computers, software, and web-based applications, including working ...

micro1 AI

Hematologist / Oncologist

Lafayette, LA · 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

New Orleans, LA · 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

Baton Rouge, LA · 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

Shreveport, LA · 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 ...

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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 Louisiana? For Clinical Trial Risk Based Monitoring jobs in Louisiana, the most frequently searched job titles are:
What job categories do people searching Clinical Trial Risk Based Monitoring jobs in Louisiana look for? The top searched job categories for Clinical Trial Risk Based Monitoring jobs in Louisiana are:
What cities in Louisiana are hiring for Clinical Trial Risk Based Monitoring jobs? Cities in Louisiana with the most Clinical Trial Risk Based Monitoring job openings:
Clinical Trial Risk Based Monitoring jobs near you

Clinician (Oncology / Hematology)

micro1 AI

New Orleans, LA • Remote

$160 - $200/hr

Part-time

This job post has expired today. Applications are no longer accepted.

Job description

Role Title: Clinician (Oncology / Hematology)


Role Type: Contractor


Location: Remote


micro1 is engaging Clinician (Oncology / Hematology)s to contribute to a customer’s project at the forefront of AI in healthcare. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review evaluation tasks that require nuanced clinical judgment, leveraging Clinical Study Reports, periodic safety reports, and regulatory correspondence in oncology and haematology.
  2. Assess the clinical defensibility of efficacy and safety conclusions, ensuring endpoints and effect sizes reflect true clinical significance.
  3. Apply advanced judgment to dose escalation, dose-limiting toxicity, modifications, adverse event grading and attribution, and the coherence of patient narratives.
  4. Evaluate benefit-risk reasoning, scrutinizing the durability of conclusions in light of new events, and the realism of described management strategies.
  5. Identify and flag content that is clinically implausible or internally inconsistent, distinguishing these from legitimate clinical variation.
  6. Provide structured, guideline-based written rationales that clearly explain the validity or limitations of clinical interpretations for a non-clinical audience.


Preferred Qualifications

  1. Specialist registration or board certification in medical oncology and/or haematology, with 5+ years of post-training clinical experience.
  2. Direct involvement in clinical trials as investigator, sub-investigator, or sponsor-side medical monitor, safety physician, or clinical development physician.
  3. Proficiency with CTCAE grading, relevant response criteria (RECIST, Lugano, IMWG, IWCLL, ELN), and outcome endpoints (ORR, DoR, PFS, OS, MRD).
  4. Hands-on experience with trial documents such as protocols, investigator brochures, CSRs, safety narratives, or DSMB/IDMC materials.
  5. Demonstrated excellence in written communication, with clear, structured explanations of clinical reasoning tailored for non-clinical readers.
  6. Previous roles in medical monitoring or as medical director on oncology or haematology programmes, and committee participation (IDMC, DSMB, adjudication, or independent review committees).
  7. Peer-reviewed publication record or authorship on clinical trial manuscripts, with any exposure to AI-assisted clinical review tools seen as a plus.

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