Sr. Project Leader

il y a 2 semaines

Paris, France Cmed Temps plein

The Aixial Group is an International Contract Research Organization (CRO), a member of the ALTEN Group, providing complex services in clinical trials (phase I-IV) and non-interventional studies. Our offices are located in France, UK, US, Belgium, Czech Republic, Switzerland, Denmark, Romania, and India.

The CRO occupies a unique position in the clinical research industry, not only as an expert in the operational delivery of clinical trials in complex disease areas including oncology, immuno-oncology, and cell therapy, but also as a developer of its own technologies for managing clinical data. This is a very exciting time to join as we are at the cutting edge, defining new and more efficient ways to design, capture, manage, review, and visualize clinical trial data.

We are currently looking for an enthusiastic and talented Senior Project Leader. This role can be home-based anywhere in the EU and will require about 10% travel.

**The Role**:
As a Senior Project Leader you will be accountable responsible for supervising and managing small to large, global, complex, full-service project(s) or multi-project programs. You'll work well alongside a team, as well as individually to plan and deliver effective implementation of clinical trials, as well as reviewing and identifying project study trends, budgets, performance metrics and project reports. You'll provide an important point of control and assurance and therefore be required to maintain a high level of leadership, problem solving and decision making.

With proven project management experience working within a CRO, Phase I studies and sound knowledge of GCP and ICH, you will have the ability to understand and interpret key business priorities. You'll be great at building relationships, an excellent communicator and will have strong interpersonal and motivational skills. You'll be managing expectations ensuring client satisfaction and will have an opportunity to have a big influence in a growing, dynamic, and successful CRO.

**Key responsibilities**:
Plan and execute multiple phase I-IV studies to agreed timelines, scope, and budget, managing all aspects including overseeing vendors, to ensure patient safety, data integrity, and adherence to contract and protocol.

**Qualifications and attributes**:
Substantial, proven experience as a Global Clinical Project Manager (required)
Study finance management experience (required)
Strong cross functional management skills (required)
Strong problem solving, organizational and time management skills. Ability to multi-task and attend to detail (required)
Therapeutic area experience in early phase oncology and immune oncology (desirable)
Contract Research Organization (CRO) background (desirable)
Strong and confident in bid defense (desirable)
Bachelor's or equivalent combination of education and experience (required)

**What we offer**:
Opportunity to be part of an innovative organization and work with exciting technologies
Mentorship and training to further develop your skills in the clinical trials industry
The chance to both lead and be part of an effective, dynamic, friendly, and supportive team
Competitive employment package

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