Remote Clinical Project Coordinator

Sumitomo Pharma

Columbia (SC)

Remote

USD 109,000 - 136,000

Full time

13 days ago
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Job summary

Sumitomo Pharma America is seeking a Clinical Trial Assistant to support the Clinical Project Manager in planning, implementation, execution, and management of multiple studies, ensuring day-to-day operations meet timelines and regulatory requirements.

This US-remote, full-time role collaborates with cross-functional teams, CROs, vendors and investigators to develop study documents, monitor data, coordinate trial supplies, and prepare updates and SOPs, with periodic on-site meetings as needed.

Qualifications

  • Bachelor's degree in a life science or related field preferred.
  • Minimum 2 years' industry experience in clinical drug development or related trials.
  • Familiarity with ICH-GCP and FDA regulations; understanding of trial conduct.

Responsibilities

  • Assist the CPM in planning, implementing, and managing multiple clinical studies.
  • Coordinate cross-functional communication to ensure proper trial execution and data quality.
  • Monitor clinical data collection and assist with site lists and CRO/vendor coordination.
  • Prepare and review study documents such as protocols, amendments and CSRs.
  • Support training, SOP updates, and trial metrics tracking.

Skills

Communication
Matrix environment
Cross-functional collaboration
Attention to detail
Problem solving
Regulatory knowledge
Team collaboration

Education

Bachelor's degree in life sciences or related field

Tools

Microsoft Office
Clinical trial systems

Job description

Sumitomo Pharma America is seeking a Clinical Trial Assistant to support the Clinical Project Manager in planning, implementation, execution, and management of multiple studies, ensuring day-to-day operations meet timelines and regulatory requirements.

This US-remote, full-time role collaborates with cross-functional teams, CROs, vendors and investigators to develop study documents, monitor data, coordinate trial supplies, and prepare updates and SOPs, with periodic on-site meetings as needed.

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