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Global Clinical Project Manager Early Phase Oncology

posted by: spj_bot

About the Job

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations/Medical Affairs. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Main Responsibilities

Job Skills

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Global Project Manager late phase oncology

posted by: spj_bot

About the Job

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations/Medical Affairs. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Main Responsibilities

Job Skills

View the job post & apply

Clinical Research Associate

posted by: spj_bot

About the Job

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Main responsibilities :

  • Ensure the proper conduct of clinical trials in oncology from initiation to close-out
  • Select investigator sites, set up studies, and monitor clinical trial progress
  • Manage and track clinical trial budgets
  • Handle required administrative tasks for study start-up and ongoing operations
  • Conduct monitoring and co-monitoring visits at investigator sites
  • Maintain regular communication with investigators and site staff
  • Review clinical trial instructions and documentation as needed
  • Prepare sites for audits and inspections, and actively participate in these processes
  • Document and track any deviations or issues observed during the study

Requirements

Job Skills

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