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Assoc. Clinical Operations Lead

Aplica ya
Mapa de ubicación: Sao Paulo, São Paulo, Brazil Full time R1220967

Descripción del trabajo

Assoc. Clinical Operations Lead

TheAssoc.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.

Requirements:

  • Bachelor Degree preferably in a life sciences discipline, and 4 years of monitoring experience, team leadership experience; or equivalent combination of education, training and experience.
  • 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.

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

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