Senior Clinical Trial Project Manager, Home-Based

Indero (formerly Innovaderm); Buenos Aires; Sur place; ARS 89 163 645 - 133 745 467; Plein temps

Avantages offerts par ce poste

Home-based position

Flexible work schedule

Ongoing learning and development

Résumé du poste

Indero is seeking a Project Manager II to lead multi-site clinical trials across dermatology and rheumatology. You will manage timelines, budgets and sponsorship communications, driving study start‑ups, TMF setup and regulatory submissions.

You will collaborate with cross‑functional teams to ensure data quality, vendor management and on‑time delivery of study deliverables, maintaining audit readiness and high standards of GCP/ICH compliance.

Qualifications

• B.Sc. in a related field of study to clinical research.
• At least 5 years industry experience and a minimum of 3 years in Phase I‑III clinical trial project management.
• Experience managing dermatology and/or rheumatology trials.
• Experience leading concurrent multi‑centered clinical trials with budgets in excess of $3M USD.
• Experience managing dermatology trials an asset.

Responsabilités

• Serve as primary contact for the Sponsor and provide timely updates on trial progress.
• Lead client calls effectively and coordinate study resources.
• Oversee preparation of study plans, protocols, eCRF, TLFs and reports.
• Plan Investigator’s Meetings and ensure site readiness with materials and budgeting.
• Collaborate with Regulatory Affairs, Data Management and other teams to meet timelines and quality standards.
• Monitor risk, budget, timelines and sponsor communications for audit readiness.

Connaissances

GCP & ICH

FDA regulations

Canadian regulations

Microsoft Office

English communication

Team collaboration

Problem solving

Organizational skills

Formation

B.Sc. in related field

Description du poste

Indero is seeking a Project Manager II to lead multi-site clinical trials across dermatology and rheumatology. You will manage timelines, budgets and sponsorship communications, driving study start‑ups, TMF setup and regulatory submissions.

You will collaborate with cross‑functional teams to ensure data quality, vendor management and on‑time delivery of study deliverables, maintaining audit readiness and high standards of GCP/ICH compliance.