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Associate Clinical Operations Lead
The Associate COL lead the execution of the Site & Patient Services (SPS) components of Real World Late Phase Research (RLWPR) studies by applying clinical research expertise, exceptional decision-making skills and innovative approaches to problem solving. Proactively set project goals and tangible expectations for SPS project team members
Essential Functions:
The Associate COL lead the execution of the Site & Patient Services (SPS) components of Real World Late Phase Research (RLWPR) studies by applying clinical research expertise, exceptional decision-making skills and innovative approaches to problem solving. Proactively set project goals and tangible expectations for SPS project team members
Essential Functions:
- Oversee the delivery of Site Management project tasks, providing advice and guidance to achieve high performance and quality project deliverables.
- Ensure overall project efficiency and adherence to project timelines and financial goals; report metrics and out of scope activities.
- Develop, implement and maintain the Site Recruitment, SPS Operations and SPS Risk Management Plan within the agreed project strategy.
- Collaborate with other functional groups within the company such as data management, quality assurance and biostatistics where necessary to support milestone achievement and to manage study issues and obstacles.
- Manage and follow study activities through ongoing tracking and review of study progress. Provide input and report progress to appropriate SPS management and project management leaders.
- Act as the first line of escalation for site management questions and issues on assigned projects.
- Lead preparation for in-house audits and in creation of Corrective Action Plans (CAPAs).
- Develop and deliver presentations/training to clients, colleagues and professional bodies, as required.
- Bachelor Degree preferably in a life sciences discipline.
- Site Manager or Monitoring experience.
- Previous leadership experience, as Lead CRA or managing Clinical Lead tasks.
- In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Skill in understanding and executing complex study designs.
- Strong written and verbal communication skills including good command of English language.
- Demonstrated team leadership and mentoring skills.
Key Skills
Ranked by relevance
gcp
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- Posted
- Jan 29, 2025
- Type
- Full-time
- Level
- Not Applicable
- Location
- Greater Buenos Aires
- Company
- IQVIA
Industries
Pharmaceutical Manufacturing
Categories
Management
Manufacturing
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3 roles aligned with this opportunity
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2026-05-27
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