The Aixial Group is an International Contract Research Organization (CRO), a member of the ALTEN Group, with offices located in France, UK, US, Belgium, Denmark, Sweden, Switzerland, Romania, and India.
The CRO occupies a unique position in the clinical research industry, supporting biotech in clinical trials across all phases (Ph. I - IV) and non-interventional studies, as an expert in the operational delivery of clinical trials. Our vision is to conduct clinical trials better than anyone else, to help patients and ultimately save lives. We have earned a strong reputation for successfully delivering complex, demanding and innovative clinical trials, with specialist therapeutic expertise in oncology, cell & gene therapy, radiopharmaceuticals and rare diseases.
We are currently looking for an enthusiastic and talented Project Leader - Contractor. This role is partially home-based in Milan area and will require up to 1.0 FTE of availability.
The Role: As a Project Leader you will be accountable 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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