About the Opportunity

The Clinical Project Manager is responsible for the management of all aspects of clinical trial activities for assigned project(s). This role is accountable for achieving successful delivery of assigned clinical trials by meeting company requirements according to time line, quality and budget.

Responsibilities

• Responsible for study commitments within the country for timely delivery of data
• Review monitoring visit reports and advise the CRAs on study related matters
• Perform any required co-monitoring & QC visits with study monitors
• Contribute to patient recruitment strategies and maintain regular communication with Investigators
• Assist in forecasting study time lines, resources, recruitment, budget & study materials
• Partner with Regulatory Affairs to ensure timely delivery of applications and documents to Regulatory Authority

Skills & Experience

• 15 years experience within clinical research in a CRO or Sponsor environment
• Strong communication skills both written and verbal
• Excellent knowledge of GCP international guidelines and relevant local regulations
• Strong background within oncology research

How to Apply

Click apply or contact Maddy Rhodes-Laird, Recruitment Consultant at MRhodes-laird@hpgconnect.com for a confidential discussion.