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Clinical Project Managers are an integral part of clinical trial delivery, working alongside
clinical teams to improve patients’ lives by bringing new drugs to the market faster.
The CPM is a member of the core project team responsible for clinical delivery of clinical studies to meet contractual requirements in accordance with Standard Operating Procedures (SOPs), policies and practices.
You will:
clinical teams to improve patients’ lives by bringing new drugs to the market faster.
The CPM is a member of the core project team responsible for clinical delivery of clinical studies to meet contractual requirements in accordance with Standard Operating Procedures (SOPs), policies and practices.
You will:
- 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 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.
- Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.
- Advanced degree or equivalent education/degree in life science/healthcare recommended.
- 7 years clinical research/monitoring experience; or equivalent combination of education, training and experience.
- At least 2-3 years leading clinical research studies (regional and/or globally speaking). Involvement in cross-functional, multicultural and international clinical trials; demonstrated capabilities in supporting operational aspects of clinical trial related activities.
- Fluent English (oral and written).
Key Skills
Ranked by relevance
gcp
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- Posted
- Mar 09, 2025
- Type
- Full-time
- Level
- Not Applicable
- Location
- Greater Buenos Aires
- Company
- IQVIA
Industries
Pharmaceutical Manufacturing
Categories
Project Management
Information Technology
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3 roles aligned with this opportunity
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2026-05-24
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View Job Details
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2026-05-20
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