Remote TMF Quality Project Manager & Records Lead

IQVIA Argentina

Bogotá

Presencial

COP 130.443.000 - 217.405.000

Jornada completa

14 días+
Generador de candidaturas

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Descripción de la vacante

IQVIA is seeking a TMF Quality Project Manager or Records Management Analyst for full home-based work in LATAM. You will coordinate TMF-related records across trials, ensuring SOP, GCP and regulatory compliance while leading project teams when needed.

You’ll manage imaging/scanning workflows, support data transfer between sites, and train staff on records-management practices to safeguard data integrity and project timelines.

Formación

  • Bachelor’s degree in Records Management or related field.
  • Minimum of four years of experience in a technically related records management environment.
  • Experience with TMF oversight, review and/or reconciliation across clinical studies.
  • Strong knowledge of ICH, GCP and applicable regulatory requirements.
  • Working knowledge of technology applications relevant to records management.
  • Ability to manage multiple tasks and projects within defined timelines.

Responsabilidades

  • Coordinate transfer, imaging, scanning, retention and disposition of project records.
  • Ensure all work complies with SOPs, policies, GCP and regulatory requirements.
  • Lead teams functionally, including scope, budgets and resources.
  • Interface with internal departments to support retrieval projects and timelines.
  • Train staff on records management policies and procedures.
  • Serve as primary point of contact for internal and external clients.
  • Oversee disposal of obsolete records and maintain storage space and equipment.

Conocimientos

Strong communication
Project coordination
Records management
English proficiency

Educación

Bachelor’s degree in Records Management or related field
Equivalent combination of education, training, and experience

Descripción del empleo

IQVIA is seeking a TMF Quality Project Manager or Records Management Analyst for full home-based work in LATAM. You will coordinate TMF-related records across trials, ensuring SOP, GCP and regulatory compliance while leading project teams when needed.

You’ll manage imaging/scanning workflows, support data transfer between sites, and train staff on records-management practices to safeguard data integrity and project timelines.

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