Global Clinical Trial Lead - Delivery, Risk & Compliance

IQVIA Argentina; Santiago; Presencial; CLP 103.189.000 - 140.713.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Sr Clinical Project Manager to lead global clinical trials from start-up through closeout. You will oversee end-to-end management, ensure compliance with GCP/ICH, and manage recruitment strategies to hit targets within a multinational framework.

The role requires extensive trial management experience and strong knowledge of regulatory requirements. IQVIA emphasizes integrity and rigorous processes across its global clinical research services.

Formación

• Bachelor's Degree Health care or other scientific discipline Req.
• Requires 8 years clinical research/monitoring experience or equivalent combination of education, training and experience.
• Minumun 3 years of regional/global trial management experience in the pharmaceutical industry or CRO.
• Requires in-depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Nice to have Cell Therapy/Hemayology TA experience.
• Requires good knowledge of project finances.
• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH and GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.

Responsabilidades

• Ensure clinical delivery of assigned projects in compliance with regulatory requirements (ICH-GCP, protocol), customer requirements (contract), and internal requirements (policies, 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 throughout the project’s lifecycle.
• Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.

Conocimientos

GCP knowledge

ICH guidelines

Clinical trial management experience

Budget/finances understanding

Cell Therapy/Hematherapy TA experience

Educación

Bachelor's Degree Health care or other scientific discipline

Minimum 3 years regional/global trial management experience

Descripción del empleo

IQVIA is seeking a Sr Clinical Project Manager to lead global clinical trials from start-up through closeout. You will oversee end-to-end management, ensure compliance with GCP/ICH, and manage recruitment strategies to hit targets within a multinational framework.

The role requires extensive trial management experience and strong knowledge of regulatory requirements. IQVIA emphasizes integrity and rigorous processes across its global clinical research services.