Innovaderm Research Inc.
Innovaderm Research Inc.
Innovaderm Research Inc. este o organizație de cercetare contractuală (CRO) axată pe dermatologie, care sprijină dezvoltarea clinică din faza I până în faza IV. Din 2000, compania colaborează cu organizații farmaceutice și din domeniul sănătății din America de Nord și Europa, oferind servicii de proiectare a studiilor, consultanță de reglementare, management de proiect, recrutarea pacienților și gestionarea datelor pentru cercetarea dermatologică.

Clinical Data Coordinator (Remote, Philippines)

Support clinical trial data management for Indero, a global dermatology and rheumatology CRO. Review, reconcile, and report clinical data while working remotely from the Philippines.

Descriere

  • Support data management activities for project teams, sponsors, and external vendors
  • Assist the Lead Data Manager with data review, reconciliation, and discrepancy resolution
  • Track study metrics and status, including enrollment and monitored or approved CRFs
  • Prepare data status updates for the project team as required
  • Produce study reports on an ad hoc basis
  • Manage user access and maintenance activities
  • Support user acceptance testing
  • Contribute to clinical database design
  • Help develop data management plans and related clinical data management documents
  • Keep data management documentation complete and current in the trial master file

Cerințe

  • Bachelor of Science degree or a related qualification
  • At least one year of clinical data management experience in the pharmaceutical industry or a CRO environment is an asset
  • Experience with an EDC system such as Medidata Rave or Medrio is an important asset
  • Comfortable using computer technology and learning new applications
  • Familiarity with CDASH and SDTM is an asset
  • Highly organized and detail-focused, with effective planning and time management abilities
  • Strong spoken and written English communication skills; French is an asset
  • Able to work in a fast-paced setting while managing competing priorities
  • Excellent interpersonal, communication, problem-solving, and organizational skills
  • Able to work effectively both independently and as part of a team
  • Understanding of drug development and relevant requirements, including Good Clinical Practice, ICH Guidelines, and Health Canada and FDA regulations or guidance
  • Legally authorized to work in the Philippines
  • Available to attend some meetings outside standard working hours, mainly in the evening

Beneficii

  • Flexible scheduling options
  • Permanent full-time employment
  • Continued learning and professional development
  • Opportunities for career advancement
  • Home-based work arrangement

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