![]() ![]() Take the next step by applying and one of our dedicated recruiters will follow up to share more details about this opportunity.We offer comprehensive medical coverage, vision care, dental and health savings accounts. ![]() If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. In addition, our best in class employee benefits, supportive poli cies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.Īt ICON, our focus is to p rovide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. Our success depends on the knowledge, capabilities a nd quality of our people. Willingness to travel up to 25% as needed.Strength in communication, planning, decision-making, negotiation, conflict management and time management skills.Subject matter expertise of working with Biotech clients.At least 2 years PM experience within clinical research and study operations.Project Management or equivalent (PMI certification) is desirable.Bachelor’s Degree in science, business, medicine or equivalent degree.Collaborate with business development to ensure we have a dedicated commercial aptitude and work together with internal colleagues and external partners to identify new avenues for growth.Report progress of projects to ICON clients and monitor and implement QC activities as necessary.Manage project study budgets and invoicing procedures according to study contract.Run a cross functional project team ensuring all necessary delivery of project training and developing a succession plan for the core team members.You have the support of extraordinary, tenured and experienced leadership whose goal is to help you apply and expand your project management, drug development and therapeutic expertise. Our projects range from phase II safety and efficacy trials to large scale outcomes mega-trials. ![]() As a Project Manager, you are involved at the forefront of innovation and drive delivery using your project leadership expertise. You will lead global trials within a therapeutically aligned team across a variety of complex indications. You will be the point of contact for designated projects, responsible to deliver successful client relationships, lead cross-functional teams, define project scope, build resource requirements, risk migration strategies, associate action plan and issue resolution. Location: Any EMEA location (Home or Office Based)Īs a Clinical Project Manager, you will expect to add towards a culture of project group excellence with a focus on process improvement, adding value and exceeding client needs. ICON people have a mission to succeed and a passion that ensures what we do, we do well Our people are our greatest strength, are at the core of our culture, and the drivin g force behind our success. With our patients at the cen tre of all that we do, we help t o accelerate the development of drugs and devices that save lives and improve quality of life. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. ICON plc is a world - leading healthcare intelligence and clinical research organisation. ![]()
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