Local Trial Manager-Canada Remote

Lensa; United States; Remote; USD 100,000 - 165,000; Full time

Job summary

Join a leading clinical research organization as a Trial Manager, where you'll oversee the execution of significant clinical studies. This role is pivotal to ensuring success through strong leadership and collaboration with cross-functional teams. With a competitive salary and commitment to inclusivity, ICON offers an engaging work environment focused on innovation and excellence in healthcare research.

Benefits

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible optional benefits

Qualifications

• Minimum 2-3 years’ experience of leading local/regional trials.

Responsibilities

• Planning and oversight of clinical study execution.
• Monitoring country enrollment and retention.
• Engaging with local functions and providing updates.

Skills

Project Management

Data Analysis

Clinical Research

Stakeholder Communication

Education

Doctorate degree

Master’s degree & 3 years of directly related experience

Bachelor’s degree & 5 years of directly related experience

Associate’s degree & 10 years of directly related experience

Job description

2 days ago Be among the first 25 applicants

Lensa is the leading career site for job seekers at every stage of their career. Our client, ICON Clinical Research, is seeking professionals. Apply via Lensa today!

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

What You Will Be Doing

• Planning,management,andoversightofclinicalstudyexecutioninaccordancewiththeglobalprogramstrategy,throughleadershipofthecross-functionalLocalStudyTeam(LST).
• Supportscountry-leveloperationalplanningandaccountableforsiteselectionwithinassignedcountry/-ies.
• Contributesanddevelopstoprogram/study-specificmaterials–e.g.,monitoringplan,studyspecifictrainingdocuments.
• SupportsandcontributestoClinicalStudyTeams(CSTs)/TrialManagementTeams(TMTs)asapplicable,agendadriven,presentatmeetings.
• Communicatescountrystatus(includingtimelinesanddeliverables)tokeystakeholders(e.g.,GlobalClinicalManagers[GCM],ProgramManagers,CSTorTMT,DevelopmentOperationsManager[DOM]etc)withoversightasrequiredandensuresupdatestorelevantsystems.
• Accountableforsite-levelgoalsettingandstudy-specificdeliverablesforclinicalsiteswithintheircountry/-ies.
• Contributesto,deliverand/orleadCRA,InvestigatorandStudyCoordinatortraining.
• Providesoversightandmonitoringofapplicablevendoractivitiese.g.,laboratoriesandequipmentprovisioning.
• Engageswithlocalclusterteamandlocalfunctionsfromastudyperspective(e.g.,Local MedicalAffairsteam,DOM)
• ProvidescountrylevelinputintotheCountryOperationalPlan(COP)andpartnerwiththeDFM throughfeasibilityandwiththeGCMstoensurelocaldeliveryofthestudy.
• ResponsibleforapprovalofBaselineandRevisedEnrolmentPlans(CountryLevel)
• Contributestothestudy-levelforecastforinvestigationalproduct,supportstudylevelaccountabilityandreconciliationacrossassignedcountries,managementofELE(enrolmentlong-rangeestimates)process.
• Monitorstheexecutionoftheclinicalstudyagainsttimelines,deliverables,andbudgetforthatcountry.
• Translatesglobalstartuprequirementsintolocalcountrytargets
• Monitorscountryenrolmentandretentionandactondeviationsfromplan.Identifybarrierstoenrolmentandsupportrecruitmentandretentionstrategicsolutions.
• Monitorsandactsupondataflowmetrics-review,trendidentificationandanalysis,withtargetedfollowupwhereappropriate.
• Monitorsandreviewscountryandstudytrends.
• ReviewsMonitoringVisitReports.
• Identifiesandfacilitatesresolutionofcross-functionalstudy-specificissues.
• Providesupdatesregardingthestudybudgetandobtainsapprovalforbudgetdeviationsforclinicalsites(outsideofrange).
• Escalatesanyissuesrelatedtodelivery,timelines,orbudgettoGCMs(orTMTleadifappropriate).
• EscalatesCRAperformanceissuestoapplicableClinicalTrialOversightManager.
• Conductson-sitequalityvisitswithCRAswhere/whenappropriateandsupportsthemaintenanceofsiterelationships.
  
  

You Are

• Doctorate degree OR
• Master’s degree & 3 years of directly related experience OR
• Bachelor’s degree & 5 years of directly related experience OR
• Associate’s degree & 10 years of directly related experience
• Minimum 2-3 years’ experience of leading local/regional trials
  
  

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
  
  

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organization. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through this form (https://careers.iconplc.com/reasonable-accommodations) .

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  IT Services and IT Consulting

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