Patient-Centric Clinical Project Manager

IQVIA; Ciudad de México; Presencial; MXN 900.000 - 1.200.000; Jornada completa

Descripción de la vacante

IQVIA in Mexico City is seeking an Associate Clinical Lead to join the core project team delivering clinical studies in line with SOPs and regulatory requirements. You will partner with Project Leaders and functional teams to ensure timely delivery and meet contractual obligations.

Responsibilities include recruitment strategy oversight, risk mitigation, financial oversight with EAC, and stakeholder communication across regions. Strong English and cross-cultural collaboration are essential.

Formación

• Requires a Bachelor's degree in health care or scientific discipline.
• 3 years clinical research/monitoring experience or equivalent.
• Knowledge of ICH/GCP regulatory guidelines.
• Broad protocol and therapeutic knowledge.
• Understanding of the Clinical Research industry and applicable environments.

Responsabilidades

• Ensure clinical delivery of projects in compliance with ICH-GCP, protocol, contract, and SOPs.
• Meet recruitment targets and implement recruitment strategies.
• Develop and manage the project risk mitigation plan and clinical risks.
• Monitor quality standards and track compliance.
• Manage Project Finances including EAC and identify opportunities beyond scope.
• Identify stakeholders and communicate with internal and external parties.
• Collaborate with the clinical team to achieve milestones and report progress.
• Lead or support the clinical team at project level across lines and countries.
• Attend site visits to support project delivery.

Conocimientos

Clinical trial delivery

Regulatory knowledge

Communication

Project coordination

Risk management

Budget/finances

Stakeholder management

Cross-cultural collaboration

Educación

Bachelor's Degree in health care or other scientific discipline

Herramientas

Microsoft Office

Descripción del empleo

IQVIA in Mexico City is seeking an Associate Clinical Lead to join the core project team delivering clinical studies in line with SOPs and regulatory requirements. You will partner with Project Leaders and functional teams to ensure timely delivery and meet contractual obligations.

Responsibilities include recruitment strategy oversight, risk mitigation, financial oversight with EAC, and stakeholder communication across regions. Strong English and cross-cultural collaboration are essential.