Senior Clinical Trial Lead — Global Biotech Studies

IQVIA; Columbia (MD); Presencial; USD 120.000 - 180.000; Jornada completa

Descripción de la vacante

IQVIA seeks a Clinical Lead to drive the clinical delivery of studies, ensuring adherence to ICH-GCP, SOPs, and contractual requirements. You will lead clinical teams, collaborate with Project Leaders, and ensure timely delivery across global trials.

The role requires 5+ years in clinical research/monitoring, strong project management and budgeting skills, and excellent communication. Eligible for on-site work in the US with potential site visits and mentorship responsibilities.

Formación

• Bachelor's degree in health care or scientific discipline.
• Requires 5 years clinical research/monitoring experience or equivalent.
• Requires basic knowledge of project management practices and terminology.
• Needs knowledge of GCP/ICH and regulatory requirements.
• Broad protocol and therapeutic knowledge.
• Understanding of clinical trial conduct and regulatory laws.

Responsabilidades

• Ensure clinical delivery of assigned projects in compliance with regulatory requirements (ICH-GCP), protocol, customer contract, and SOPs.
• Meet recruitment targets with appropriate recruitment strategies.
• Develop risk mitigation plans and manage clinical risks throughout the project lifecycle.
• Ensure quality delivery by identifying and monitoring quality standards and issues.
• Manage project finances, including Estimate at Completion (EAC), and identify opportunities for scope changes.
• Identify clinical stakeholder landscape and manage internal and external stakeholders.

Conocimientos

Clinical Delivery

Project Management

GCP/ICH regulatory knowledge

Leadership/Mentoring

Communication

Budgeting/Finance understanding

Educación

Bachelor's Degree in health care or scientific discipline

Herramientas

Microsoft Word

Excel

PowerPoint

Descripción del empleo

IQVIA seeks a Clinical Lead to drive the clinical delivery of studies, ensuring adherence to ICH-GCP, SOPs, and contractual requirements. You will lead clinical teams, collaborate with Project Leaders, and ensure timely delivery across global trials.

The role requires 5+ years in clinical research/monitoring, strong project management and budgeting skills, and excellent communication. Eligible for on-site work in the US with potential site visits and mentorship responsibilities.