LogoFresh Jobs Ahead
IQVIA
IQVIA
H1B Visa SponsorConsultingManufacturingMarketing
IQVIA combines healthcare data analytics, advanced technology, and consulting to help organizations address complex challenges across the life sciences and healthcare sectors. Its Connected Intelligence platform brings together data and artificial intelligence to support clinical research, technology development, and the advancement of new therapies. The company’s teams work across analytics, consulting, and healthcare technology, offering opportunities connected to research, digital innovation, and efforts to improve patient outcomes.
LinkedIn
Company Jobs

Clinical Research Associate - Hybrid in Melbourne

Support clinical trial sites and study data for IQVIA in Australia. The role covers recruitment, compliance, documentation, monitoring, and trial delivery.

AUAustraliaHybridFull-timeJuniorMiddleEnglish RequiredClinical Research
Google Cloud Platform

Description

  • Oversee site monitoring and management to ensure study conduct and data reporting meet protocols, regulations, guidelines, and sponsor requirements.
  • Conduct site visits across selection, initiation, monitoring, and close-out stages.
  • Implement, advance, and monitor subject recruitment plans.
  • Deliver protocol and study training to assigned sites while maintaining regular site communication.
  • Assess site practices for protocol and regulatory compliance, escalating quality concerns as needed.
  • Monitor regulatory submissions, approvals, recruitment, enrollment, CRF completion, and the creation and resolution of data queries.
  • Assist with study start-up activities when required.
  • Maintain Trial Master File documentation and confirm that Investigator Site Files are properly maintained.
  • Record site-management activities, monitoring findings, and action plans in visit reports and follow-up correspondence.
  • Work with study team members to support project delivery.
  • Help create site-specific subject recruitment plans when required.
  • Oversee site finances and collect invoices in line with local requirements when required.

Requirements

  • Bachelor’s degree in a scientific or healthcare discipline, or an equivalent combination of education, training, and experience.
  • At least nine months of independent on-site monitoring experience.
  • Working knowledge of clinical research regulations, including GCP and ICH guidelines.
  • Working therapeutic-area and protocol knowledge gained through company training.
  • Proficiency with Microsoft Word, Excel, and PowerPoint.
  • Ability to use a laptop, iPhone, and iPad when required.
  • Strong organizational and problem-solving abilities.
  • Effective time and financial management skills.
  • Ability to build and maintain productive relationships with colleagues, managers, and clients.

Benefits

  • Competitive salary plus car and health allowances.
  • Flexible hybrid working arrangement.
  • Career development opportunities across FSO and FSP models.
  • Opportunity to work with experienced managers across clinical trials in multiple phases.

Related Jobs

Kreato Global | BPO and Language Solutions

Remote English-Spanish OPI/VRI Interpreter

Kreato Global | BPO and Language Solutions
201 – 500 Employees
HealthcareHospitalityLogistics
ARArgentinaBOBoliviaBRBrazilCLChileCOColombiaCRCosta RicaCUCubaDODominican RepublicECEcuadorGTGuatemalaHNHondurasHTHaitiMXMexicoNINicaraguaPAPanamaPEPeruPRPuerto RicoPYParaguaySVEl SalvadorUYUruguayVEVenezuelaRemoteFull-timeJuniorNo degree requiredEnglish RequiredSpanish RequiredTranslator

Interpret remotely between English- and Spanish-speaking people in medical, financial, social service, and customer care settings. Provide language support for Kreato Global across Latin America.

Open