Senior Global Trial Manager – Oncology, Remote/Home-Based

IQVIA Inc; Quilmes; Remote; ARS 131,359,000 - 185,448,000; Full time

Job summary

IQVIA Biotech is seeking a Clinical Trial Manager II to oversee the clinical delivery of studies from initiation to closeout. The role involves coordinating with clinical teams to ensure timelines, quality, and regulatory compliance across multiple sites and geographies.

The position requires collaboration with Project Leaders and cross-functional teams to ensure projects meet contractual and SOP requirements, while driving efficient recruitment and risk mitigation strategies across trials.

Responsibilities

• Ensure clinical delivery of assigned projects in compliance with ICH-GCP, protocol, contract and SOPs.
• Meet recruitment targets and implement appropriate recruitment strategies.
• Contribute to risk mitigation plans and manage clinical risks throughout the project.

Job description

Clinical Trial Manager II, IQVIA Biotech

Mexico City, Mexico
Buenos Aires, Argentina
Mexico City, Mexico
Columbia, Maryland, United States of America
Full time
R
alongside clinical teams to improve patients' lives by bringing new drugs to the market faster. The Clinical Lead is a member of the core project team responsible for the clinical delivery of clinical studies to meet contractual requirements in accordance with Standard Operating Procedures (SOPs), policies and practices. Clinical Leads ensure clinical delivery to customers, lead clinical teams and partner with Project Leaders and other functional teams ensuring projects meet delivery requirements at all times.

Essential Functions

• Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).
• Accountable for meeting projects' recruitment targets and ensuring appropriate recruitment strategies are in place.
• Contribute to the development of the project risk mitigation plan and manage clinical risks through the project's