Global Clinical Project Manager, Early Hematology - Remote

Overview

We currently have an exciting new opportunity for an experienced Global Clinical Project Manager within the Early Hematology team to join a successful sponsor dedicated program. We are looking for a Global Clinical Project Manager which is a business-critical role within Study Management, BioPharmaceuticals Clinical Operations, whose main accountability is the project delivery of clinical studies.

The Global Clinical Project Manager is responsible for leading a cross-functional study team and for providing the team with direction and guidance to enable successful study delivery. The Global Clinical Project Manager is the main liaison between the study team and the Clinical Program Team (CPT) starting with study handover through to close-out and archiving. The Global Clinical Project Manager is accountable to the CPT for the delivery of a study according to agreed upon timelines, budget, and quality standards by ensuring an effective partnership and teamwork within study team and/or external partners.The Global Clinical Project Manager leads the study team and/or study oversight team in accordance with the study team operating model, current clinical trial regulations (e.g. ICH GCP).

Must have strong cross functional management, Vendor management and full oversight, budget management, managed the full project oversight across globally.

This is a permanent role with ICON on FSP and fully home-based. You must be located in the following countries to be consider: Poland, Spain.

In Short

• Lead a cross-functional study team for clinical studies.
• Ensure study delivery according to timelines, budget, and quality standards.
• Act as the main liaison between study team and Clinical Program Team.
• Manage vendor relationships and ensure contracted goals are met.
• Conduct investigator meetings and develop essential study documents.
• Oversee study level performance and communicate risks.
• Ensure compliance with clinical research regulations.
• Manage study budget and provide progress reports.
• Identify and report quality issues within the study.
• Ensure Trial Master File completeness.

Requirements

• University degree in medical or biological sciences or clinical research.
• 5 years of relevant clinical experience in the pharmaceutical industry.
• 2 years of global project management experience.
• Project management certification.
• Extensive knowledge of ICH-GCP and clinical study management.
• Strong project management and leadership skills.
• Excellent communication and interpersonal skills.
• Strong organizational and problem-solving abilities.
• Ability to manage competing priorities.
• Current experience in clinical research within a Pharma or CRO setting.

Benefits

• Opportunity to work in a dynamic and supportive environment.
• Engage in impactful clinical research projects.
• Flexible working conditions.
• Competitive salary and benefits package.
• Professional development opportunities.