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Clinical Trial Risk Based Monitoring Jobs in Virginia

Alcanza

Clinical Research Site Manager

Fredericksburg, VA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Reviewing the performance dashboards and other clinical trial systems to oversee site and patient ... Employing problem-solving skills to propose and implement risk mitigations; * Participating and ...

Patterns Hiring, Inc.

Clinical Nurse

Fairfax, VA · On-site

Clinical trial experience preferred Essential Duties and Responsibilities: Essential and other ... Ensures evidence-based symptom management as permitted by the protocol * Patient health counseling ...

Marmon

Compliance Business Partner

Charlottesville, VA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

Design and perform risk-based monitoring activities, such as field rides, review of HCP engagements ... Experience advising commercial, marketing, medical education, scientific, clinical, R&D, regulatory ...

IQVIA Holdings

Clinical Nurse

Fairfax, VA · On-site

Current Registered Nursing License for the state the role is based in for RN's * Oncology experience preferred * Clinical trial experience preferred Why Join Us? At NEXT Oncology (an Avacare Business ...

IQVIA, Inc.

Clinical Nurse

Fairfax, VA · On-site

Current Registered Nursing License for the state the role is based in for RN's * Oncology experience preferred * Clinical trial experience preferred Why Join Us? At NEXT Oncology (an Avacare Business ...

IQVIA

Clinical Nurse

Fairfax, VA

Current Registered Nursing License for the state the role is based in for RN's * Oncology experience preferred * Clinical trial experience preferred Why Join Us? At NEXT Oncology (an Avacare Business ...

IQVIA

Clinical Nurse

Fairfax, VA

Current Registered Nursing License for the state the role is based in for RN's * Oncology experience preferred * Clinical trial experience preferred Why Join Us? At NEXT Oncology (an Avacare Business ...

IQVIA

Clinical Nurse

Fairfax, VA · On-site

Current Registered Nursing License for the state the role is based in for RN's * Oncology experience preferred * Clinical trial experience preferred Why Join Us? At NEXT Oncology (an Avacare Business ...

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All JobsClinical Trial Risk Based Monitoring JobsClinical Trial Risk Based Monitoring Jobs in Virginia

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.

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.

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

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

Clinical Trial Risk Based Monitoring jobs near you

Clinical Research Sub-Investigator (MD)

RE:Cognition Health, Inc

Fairfax, VA • On-site

Full-time

Re-posted 10 days ago

Job description

Company Description
Re:Cognition Health is a pioneering brain and mind clinic.
We specialize in the treatment and care of people showing symptoms of cognitive impairment or mental health concerns. Using the latest progressive medical research and evidence based treatments we are passionate about transforming and optimising cognitive performance through education, clinical excellence and by providing access to emerging treatments.The Re:Cognition Clinics are major centers for international trials of disease-modifying and new symptomatic drugs for Alzheimer's disease and other neurological conditions.
Join a team that is a Global leader in clinical trials and dedicated to providing World-class Medical Care
Job Description
Unique opportunity to join a fast growing clinical trial research team in the field of cognitive impairment as a Sub-Investigator. This is a full-time, regular position, working in the clinic from 9:00 to 5:30 pm Monday - Friday, with occasional hours outside this time frame to meet participant needs. You will work with a cutting-edge team dedicated to ensuring the future is better. To be accepted as an applicant for this position you must have a current license to practice as Medical Doctor in the Commonwealth of Virginia, or be able to attain the licensure within 4 weeks of offer.
Responsibilities include:
  • Complete of training on specific rating scales prior to the commencement of any study procedures
  • Perform clinical safety assessments and monitoring for study trial participation to include such items as: physical exams, EKG's, phlebotomy and lab work evaluation
  • Administer study drug(s), per protocol including placing and monitoring IV infusions
  • Perform lumbar punctures per the direction of the protocol and Principal Investigator
  • Recruit clinical protocol participants
  • Apply knowledge of center's clinical protocols for the care of study participants

The ideal individual is a dedicated clinical practitioner with experience in cognitive disease and clinical research. This is a role that requires an individual who is capable and willing to perform both clinical and research related duties. This position is an intricate research team, must be self-directed and have the ability to interact with multi discipline team and while maintaining the safety of the study participants and their families.
Qualifications
Medical Doctor (MD) with current license to practice in Virginia
Current CPR Certification
Ability to follow HIPAA regulations in regards to patient confidentiality
Ability to pass a Background Check Investigation including Drug Screen
Additional Information
All your information will be kept confidential according to EEO guidelines.
https://www.recognition.health/

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