Remote Contract Negotiator, Clinical Research (Argentina)

IQVIA Inc; Buenos Aires; Remote; ARS 1,200,000 - 1,800,000; Full time

Job summary

IQVIA is seeking a Contract Specialist to join the Country Site Activation team in Argentina. This remote, home-based role focuses on country-level site activation activities, contract negotiations with clinical research sites, and ensuring regulatory compliance.

You will act as the SPOC for sites, SAMs, and PM teams, coordinating startup activities, documentation, and timelines. A Health Sciences degree and 2+ years in clinical research are required, with strong English proficiency.

Qualifications

• 2+ years of clinical research experience in contract negotiations
• Advanced English required
• Knowledge of GCP/ICH and regulatory guidelines
• Desirable experience in regulatory submissions & imports/exports
• Excellent organization and communication skills

Responsibilities

• Perform country-level Site Activation (SA) tasks per local/international regulations and SOPs.
• Serve as SPOC for investigative sites, SAM, PM team, and other departments.
• Ensure SOP/WIs compliance and timely deliverables and project timelines.
• Negotiate contracts with research sites.
• Execute startup and site activation per regulations and share documents with sites and team.
• Maintain accuracy of internal systems and project data.
• Track progress, approvals, and execution of regulatory/ethics/ICF/IP release documents.
• Provide local expertise during project planning with SAMs and teams.
• Quality control of documents provided by sites.
• May liaise with sponsors on specific initiatives.

Skills

Clinical research

Contract negotiations

GCP/ICH knowledge

English proficiency

Regulatory submissions

Communication skills

Education

Health Sciences degree

Job description

IQVIA is seeking a Contract Specialist to join the Country Site Activation team in Argentina. This remote, home-based role focuses on country-level site activation activities, contract negotiations with clinical research sites, and ensuring regulatory compliance.

You will act as the SPOC for sites, SAMs, and PM teams, coordinating startup activities, documentation, and timelines. A Health Sciences degree and 2+ years in clinical research are required, with strong English proficiency.