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Clinical Trial Risk Based Monitoring Jobs in Pennsylvania

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Clinical Trial Liaison

Blue Bell, PA

$110K - $138K/yr

... based research initiatives etc * Capture and elevate critical insights from sites to optimize ... Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data ...

ICON

Clinical Trial Liaison

Blue Bell, PA · On-site +1

$110K - $138K/yr

... based research initiatives etc * Capture and elevate critical insights from sites to optimize ... Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data ...

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Clinical Trial Liaison

Blue Bell, PA · On-site

$110K - $138K/yr

... based research initiatives etc * Capture and elevate critical insights from sites to optimize ... Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data ...

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Clinical Trial Manager

Philadelphia, PA · On-site

Participate in or lead set-up and implementation of effective investigator and site monitor ... based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package ...

New

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Clinical Trial Liaison

Blue Bell, PA · On-site

$110K - $138K/yr

... based research initiatives etc * Capture and elevate critical insights from sites to optimize ... Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data ...

ICON

Clinical Trial Liaison

Blue Bell, PA · On-site +1

$110K - $138K/yr

... based research initiatives etc * Capture and elevate critical insights from sites to optimize ... Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data ...

ICON

Clinical Development Trial Lead

Blue Bell, PA · On-site +1

Risk - Assess, identify and monitor trial-level risks. Incorporate scientific knowledge, trial ... Identify and assist in developing continuous improvement activities based on important trends such ...

ICON

Clinical Development Trial Lead

Center Square, PA · On-site

$120 - $190/hr

Risk - Assess, identify and monitor trial‑level risks. Incorporate scientific knowledge, trial ... Identify and assist in developing continuous improvement activities based on important trends such ...

New

Novocure

Clinical Trial Lead

Wayne, PA · Hybrid

$147K - $190K/yr

Oversee study timelines, milestones, deliverables, and risk mitigation plans. * Manage study ... Monitor CRO and vendor performance to ensure quality and compliance. * Support protocol development ...

Novocure

Clinical Trial Lead

Philadelphia, PA · Hybrid

$147K - $190K/yr

Oversee study timelines, milestones, deliverables, and risk mitigation plans. * Manage study ... Monitor CRO and vendor performance to ensure quality and compliance. * Support protocol development ...

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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.
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Clinical Trial Risk Based Monitoring jobs near you

Clinical Trial Liaison

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Blue Bell, PA

$110K - $138K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 18 days ago

Job description

Clinical Trial Liaison - Mid- Atlantic

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.


As a Clinical Trial Liaison at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What you will do:

Clinical Investigator Management

  • Accountable for the full spectrum of investigator engagement from identification and qualification through enrollment, and support database lock, and study closeout

  • Serve as a clinical trial scientific ambassador, ensuring investigators deeply understand protocol intent, scientific rationale, and patient eligibility requirements

  • Develop and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas

  • Influence enrollment by co-creating tailored recruitment strategies aligned with site capabilities, patient population realities, and study objectives

  • Proactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites, including for example, novel site models, community-based research initiatives etc

  • Capture and elevate critical insights from sites to optimize feasibility, protocol design, and study conduct

Clinical Trial Management

  • Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery

  • Leverage performance metrics to anticipate issues, intervene decisively, and maintain momentum toward clinical milestones

  • Drive inspection readiness as a continuous discipline across sites

  • Collaborate across functions and with vendor partners to resolve operational barriers, ensuring delivery with speed and quality

  • Maintain advanced understanding of local treatment paradigms and standard of care to influence strategic country/site selection and protocol localization

  • Provide oversight and quality assurance for vendor monitoring, escalating risks proactively

  • Where applicable, lead end-to-end management of Post-Marketing Safety Studies in compliance with local regulations

  • Business Management and Engagement

  • Cultivate a portfolio of strategically aligned, high-impact investigators who consistently prioritize client trials

  • Enable an exceptional investigator experience by being a responsive, knowledgeable, and valued scientific partner

  • Collaborate cross-functionally (e.g., Medical, Clinical, Study Delivery) to align on trial and site priorities, troubleshooting challenges with urgency and creativity

  • Conduct data-informed site prospecting and prioritization, contributing to trial competitiveness and regional strategic execution

  • Maintain scientific fluency and therapeutic expertise to lead meaningful, solutions-focused discussions with site personnel

  • Act as a key liaison between field teams, vendors, and investigators, ensuring alignment, shared purpose, and continuous knowledge transfer

  • Partner closely with field team colleagues to elevate the investigator and site experience, ensuring seamless collaboration and improving enrollment outcomes and Investigator relationships


You are:

  • Bachelor's degree or equivalent; strong preference for scientific, clinical, or health-related fields

  • Minimum 5 years of experience in clinical research or pharmaceutical industry with experience directly interacting with or working with HCPs and clinical sites

  • Open to up to 60-80% travel during peak times (travel will vary)

  • Oncology experience required (Breast/Gyn experience preferred)

  • Location: Mid-Atlantic, Southeast Region


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.

Salary Range

$110,520.00-$138,150.00

Are you a current ICON Employee? Please click here to apply

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