Global Project Manager    Office based in Brussels - Belgium Relocation bonus available ! Extensive Oncology Experience is a must  4 years or above experience on Global Project Management (not only in one region but global) Open for candidates from EU who wants to relocate to Brussels - Belgium  (Bulgaria, Greece, Germany, France, Italy, Austria, Netherlands, Poland )  

For our client, a global pharmaceutical organization we are currently looking for a Global Clinical Project Manager (phase II/III Oncology studies).  

As a Global Project Manager, you will independently lead and oversee multiple global clinical trials and operations for cross-functional study team(s).

You will lead and oversee protocols at program level and you are responsible for data listing review, external vendor contracting and oversight of CRO Teams, external laboratories, scans.

You will have the strategic oversight of the study including risk and issue identification and planning, matrix management of assigned study team members, global project management. And you will act as a matrix leader for the global clinical operations team and are accountable for the timely execution of the specific tasks within the protocols or programs.

The ideal candidate has:

• At least a minimum of 8 years of experience in the pharmaceutical or related industries.
• Minimum education BA/BS.
• Proven global clinical trial management activities: i.e. experience in aspects of clinical trial management including study start-up, enrollment, maintenance, closeout, regulatory obligations, vendor oversight, and data listing review, adverse event reporting, and budget management.
• Demonstrates global project management skills including project planning and prioritization, timeline management, time and meeting management skills, and ability to identify and appropriately manage or escalate risks.
• Innovative problem solving at global level.
• Ability to form positive working relationships with team members and stakeholders through effective communication, collaboration, and expectation setting.
• Understanding of ICH/GCP Guidelines and local regulatory guidelines or regulations; knowledge of clinical trial conduct; knowledge of the pharmaceutical industry and of the pre-clinical, clinical, regulatory and commercial components.
• Effective oral, written and interpersonal communication skills.
• Proven experience with conflict and issue management.
• Demonstrated ability to multi-task and manage high performance demands.

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