Remote Senior Clinical Trials Associate

Worldwide; Buenos Aires; Híbrido; ARS 90.547.000 - 135.820.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials is seeking a Senior Clinical Trials Associate to provide administrative and project tracking support to the clinical project team. You will arrange access, audit documents, manage Investigator Site Files, and ensure accurate trial master file versioning.

The role requires a degree or equivalent experience with at least two years in a related field, plus strong English skills and Spanish fluency for Argentina.

Formación

• Degree level qualification or equivalent experience plus a minimum of two years’ experience in a related role.
• Excellent written and verbal English is required; Spanish language fluency is expected for Argentina.
• Strong interpersonal, organizational and problem-solving abilities.

Responsabilidades

• Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.).
• Maintain and quality audit to assure the most recent revisions of documents are on project portals.
• Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File.
• Maintain version and quality control of project documentation and submit to trial master file.
• Assist with tracking and maintenance of project related information, including site medical question and answer log.
• Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management.

Conocimientos

Excellent written English

Verbal English

Spanish language fluency

Interpersonal skills

Attention to detail

Organizational skills

Problem-solving skills

Educación

Degree level qualification or equivalent experience

Descripción del empleo

Worldwide Clinical Trials is seeking a Senior Clinical Trials Associate to provide administrative and project tracking support to the clinical project team. You will arrange access, audit documents, manage Investigator Site Files, and ensure accurate trial master file versioning.

The role requires a degree or equivalent experience with at least two years in a related field, plus strong English skills and Spanish fluency for Argentina.