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Clinical Trial Risk Based Monitoring Jobs in Connecticut

Insight Global

Clinical Trial Support RN

New Haven, CT · On-site

$50 - $55/hr

... extensions based on calendar year PR: $50-$55 per hour Interview Process: 1 and done in-person ... You will also monitor and report on the safety and efficacy of the vaccine candidates, provide ...

Novotech

Clinical Lead

Brooklyn, CT · On-site

... trial. They do this by ensuring high quality site selection, review and approval of monitoring ... Develop and distribute Site Initiation Visit (SIV) materials based on materials provided from the ...

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Clinical Trial Risk Based Monitoring information

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.

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 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 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 are popular job titles related to Clinical Trial Risk Based Monitoring jobs in Connecticut?

For Clinical Trial Risk Based Monitoring jobs in Connecticut, the most frequently searched job titles are:

What job categories do people searching Clinical Trial Risk Based Monitoring jobs in Connecticut look for?

The top searched job categories for Clinical Trial Risk Based Monitoring jobs in Connecticut are:

What cities in Connecticut are hiring for Clinical Trial Risk Based Monitoring jobs?

Cities in Connecticut with the most Clinical Trial Risk Based Monitoring job openings:

Clinical Trial Risk Based Monitoring jobs near you

Clinical Trial Support RN

Insight Global

New Haven, CT • On-site

$50 - $55/hr

Contractor

Medical, Dental, Vision, Life

Posted 16 days ago

Job description

Insight Global is looking to hire RN Clinical Trail Support Staff for a top national healthcare client in New Haven, CT!

Location: 1 Howe Street, New Haven, CT 06511

Duration: 24 month contract, indefinite extensions based on calendar year

PR: $50-$55 per hour

Interview Process: 1 and done in-person interview

Hours:

  • The working hours are 1st and 2nd shift with some flexibility with the ability to work 4 weekend shifts a month along with holidays

Must Haves:

  • 5 years of clinical experience as an RN
  • Registered NurseExperience taking vitals, overseeing meals as data, blood draws, EKG/ECG, working with clinical coordinators/project managers, working with pharmacy/lab/front deskExperience with Discharge planning

Day to Day:

Insight Global is looking for clinical trial support staff to join our vaccine development team at a large pharmaceutical company in New Haven, CT. As a clinical trial support staff member, you will be responsible for coordinating and conducting clinical trials for new vaccine candidates, ensuring compliance with protocols, regulations, and ethical standards. You will also monitor and report on the safety and efficacy of the vaccine candidates, provide education and support to trial participants, and collaborate with other health professionals and researchers. To be successful in this role, you will need any of the following: an RN license, and at least 3-5 years of experience in a clinical setting. You will also need excellent communication, organizational, and problem-solving skills, as well as a passion for advancing public health through innovation.

The working hours are 1st and 2nd shift with some flexibility with the ability to work 4 weekend shifts a month along with holidays. This individual will be brought on to support vaccine development in human patients but will eventually move on to different projects once the vaccine development is completed.


Compensation:

$50 - $55 per hour


Exact compensation may vary based on several factors, including skills, experience, and education.