Added
9 hours ago
Type
Full time
Salary
Salary not provided

Related skills

sharepoint oncology ctms microsoft project hematology

📋 Description

  • Organizes and participates in Monitor’s and Investigator’s Meetings.
  • Performs co-monitoring visits for assigned projects.
  • Monitors sites for assigned projects after training.
  • May act as Feasibility Associate after training.
  • Review and approve third-party invoices and contractor timesheets.
  • Develop and implement solutions to issues affecting timelines, resources, budgets.

🎯 Requirements

  • University Degree in scientific, medical or paramedical disciplines.
  • 3+ years PM experience in CRO/Pharma or 6+ years as CM/CRA.
  • Excellent knowledge of clinical trial operations, GCP/ICH guidelines and regulatory requirements.
  • Experience managing complex oncology and hematology studies.
  • Excellent English communication skills: written and verbal.
  • Proficient in Word, Excel, PowerPoint, MS Project, SharePoint; travel required.

🎁 Benefits

  • Permanent remote opportunity with potential hybrid arrangement.
  • Global team across pharma, biotech, devices.
  • Work on oncology and hematology clinical trials.
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