Clinical Coordinator

Aviso de fuente externaen Insight Global

12 Month Contract - full time 40/hrs a Week Fully remote - Colombia - Ideally based in BogotaHourly Rate $5-6/USD/ hour Clinical Studies Support Coord III (Remote, Bogota): The clinical o...

Fuente externa - sin verificarayerVigente hasta: 18 sep 2026

Salario

No especificado

Ubicación

Bogotá, Colombia

Tipo de empleo

Tiempo completo

Modalidad

No especificado

Clinical Coordinator

Bogotá, Colombia

Descripción del empleo

12 Month Contract - full time 40/hrs a Week Fully remote - Colombia - Ideally based in BogotaHourly Rate $5-6/USD/ hour
Clinical Studies Support Coord III (Remote, Bogota):
The clinical operations support/coordinator position that helps keep clinical trials organized, compliant, and running smoothly.
The person acts as the administrative and operational backbone of clinical studies by managing study documentation, data quality, contracts, compensation tracking, system updates, and communication among stakeholders.
Responsibilities may include:
Supports clinical studies by executing and maintaining one or more areas.Data coordination: participates in development/testing of case report forms, study reports, and study databases based on protocol requirements.Ensures timely and quality completion of data forms; verifies study data; generates/manages/resolves data discrepancies.May process compensation and identify/resolve compensation discrepancies.Document coordination creates/manages clinical study files; oversees organization and distribution of clinical study documents.Assists with periodic audits of clinical study files for completeness and accuracy.Ensures study contracts are tracked, renewed or sent to legal when an amendment or other review is necessary.Supports shipment/delivery of study products to hospitals as needed for research activities.Updates study manager on any issues with legal and compliance reviews as projects move through the approval and enrollment phases.Maintains training on SOP's, and various systems such as: Veeva, ONIT, IdeaPoint and others.Must be fluent in English, Spanish. Portuguese also preferred.2 Years in a clinical research settingCollege Degree
Day to Day:
Clinical trials generate a massive amount of data and documentation. This coordinator ensures:
Study data is entered correctlyMissing or incorrect data gets resolvedClinical trial files stay organized and audit-readyContracts are tracked and renewedStudy products reach hospitals when neededCompliance and legal approvals move through the processStudy teams stay informed of any issues

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