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Clinical Research Supervisor

  • ... Posted on: Feb 19, 2026
  • ... Medix™
  • ... East Brunswick, New Jersey
  • ... Salary: Not Available
  • ... Full-time

Clinical Research Supervisor   

Job Title :

Clinical Research Supervisor

Job Type :

Full-time

Job Location :

East Brunswick New Jersey United States

Remote :

No

Jobcon Logo Job Description :

OverviewWe are seeking a highly organized and experienced On-site Clinical Research Supervisor to lead oncology clinical trial operations within a growing research organization. This individual will oversee Clinical Research Coordinators, ensure compliance with regulatory and protocol requirements, and serve as a key liaison between sponsors, regulatory bodies, and internal teams.The ideal candidate brings strong leadership experience, hands-on oncology trial expertise (Phase II–IV interventional studies), and a commitment to operational excellence and patient-centered care.Key ResponsibilitiesSupervise and mentor Clinical Research Coordinators, optimizing workload distribution and performanceEnsure strict adherence to study protocols, GCP, regulatory, and institutional requirementsLead site qualification, initiation, monitoring, and close-out visitsReview and interpret study protocols, informed consent forms, and safety documentation with staffOversee subject screening and enrollment to ensure eligibility criteria are metEnsure protocol-compliant execution of all study visits, assessments, and proceduresManage investigational product (IP) inventory, accountability, and reconciliationOversee accurate and timely data collection and entry into sponsor systemsAct as primary liaison with sponsors, monitors, and regulatory representativesLead review and implementation of protocol amendments and safety updatesSupport sponsor audits, FDA inspections, and internal quality reviewsConduct feasibility assessments and assist with enrollment strategies as neededMaintain high standards of professionalism, confidentiality, and patient careRequired QualificationsMinimum 5 years of clinical research experienceExperience outside of an academic/institutional settingPrior experience in a Supervisor or Manager roleStrong background in interventional oncology trials (Phase II–IV)ScheduleM - F, 8 A.M. - 5 P.M.Sometimes flexible depending on trialsPreferred QualificationsExperience managing an Oncology Research Site within an industry settingWhy Join Us?Be part of a growing organization with strong development potentialLeadership opportunity with direct impact on oncology research operationsCollaborative, patient-focused environmentOpportunity to shape processes and drive operational excellence

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Jobcon Logo Position Details

Posted:

Feb 19, 2026

Employment:

Full-time

Salary:

Not Available

City:

East Brunswick

Job Origin:

APPCAST_CPC

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OverviewWe are seeking a highly organized and experienced On-site Clinical Research Supervisor to lead oncology clinical trial operations within a growing research organization. This individual will oversee Clinical Research Coordinators, ensure compliance with regulatory and protocol requirements, and serve as a key liaison between sponsors, regulatory bodies, and internal teams.The ideal candidate brings strong leadership experience, hands-on oncology trial expertise (Phase II–IV interventional studies), and a commitment to operational excellence and patient-centered care.Key ResponsibilitiesSupervise and mentor Clinical Research Coordinators, optimizing workload distribution and performanceEnsure strict adherence to study protocols, GCP, regulatory, and institutional requirementsLead site qualification, initiation, monitoring, and close-out visitsReview and interpret study protocols, informed consent forms, and safety documentation with staffOversee subject screening and enrollment to ensure eligibility criteria are metEnsure protocol-compliant execution of all study visits, assessments, and proceduresManage investigational product (IP) inventory, accountability, and reconciliationOversee accurate and timely data collection and entry into sponsor systemsAct as primary liaison with sponsors, monitors, and regulatory representativesLead review and implementation of protocol amendments and safety updatesSupport sponsor audits, FDA inspections, and internal quality reviewsConduct feasibility assessments and assist with enrollment strategies as neededMaintain high standards of professionalism, confidentiality, and patient careRequired QualificationsMinimum 5 years of clinical research experienceExperience outside of an academic/institutional settingPrior experience in a Supervisor or Manager roleStrong background in interventional oncology trials (Phase II–IV)ScheduleM - F, 8 A.M. - 5 P.M.Sometimes flexible depending on trialsPreferred QualificationsExperience managing an Oncology Research Site within an industry settingWhy Join Us?Be part of a growing organization with strong development potentialLeadership opportunity with direct impact on oncology research operationsCollaborative, patient-focused environmentOpportunity to shape processes and drive operational excellence

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