Industry: Pharmaceuticals & Biotech•
5 - 7 years
Posted 105 days ago
Do you think you have what it takes to be a part of a successful study delivery team? ICON’s award-winning study execution capabilities have led to the approval of 18 of the world’s top 20 best-selling drugs. Make your experience count for the benefit of patients worldwide!
Location: Any US location (Home or Office Based)
As part of our Oncology & Haematology Project Management Group you will be leading global trials across a wide range of indications within a therapeutically aligned team. With us you will be at the forefront of innovation, working onprojects in translational medicine, immuno-oncology, epigenetics and more, with opportunity to support First-in-Human and First-in-Class drug trials. Our adaptive design expertise underpins our ability to accelerate delivery of new therapies to patients and will broaden your experience in this exciting field. At ICON you will be supported in applying and expanding your project management, drug development and therapeutic expertise!
Manage a cross functional project team ensuring all necessary project training is provided and developing a succession plan for the core team members. Manage projects in accordance with the contract including: study budget, study invoicing procedures, monitoring and reporting on progress of projects to stakeholders and implementing QC activities as necessary. Collaborate with business development to ensure proactive commercial aptitude while partnering withinternal and external stakeholders to identify new avenues for growth.
Benefits of Working in ICON:
ICON provides Project Manager’s with the innovative resources to be successful in delivering results, inspiring others and becoming a trusted partner. We offer an exceptional benefits package that includes a comprehensive health plan, retirement plans, highly competitive pay, corporate bonus plan, 5+ weeks PTO, and many other incentives amongst an opportunity to grow your career within ICON!
Bachelor’s Degree in medicine, science or equivalent degree and a qualification in Project Management or equivalent (PMI certification) are desirable. At least 4 years PM experience and 6 years within clinical research operations is essential. Specific therapeutic experience within internal medicine indications and comprehensive knowledge of ICH-GCP is essential along with excellent communication, planning, decision-making, negotiation, conflict management and timemanagement skills. Willingness to travel up to 25% as needed.
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able toprovide you with more details about this opportunity.