Innovaderm Research Inc.
Innovaderm Research Inc.
Innovaderm Research Inc. is a dermatology-focused Contract Research Organization (CRO) that supports clinical development from Phase I through Phase IV. Since 2000, the company has worked with pharmaceutical and healthcare organizations across North America and Europe, providing study design, regulatory consulting, project management, patient recruitment, and data management for dermatology research.

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.

Description

  • 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

Requirements

  • 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

Benefits

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

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