Group Manager, Interactive Technologies - Raleigh, North Carolin

TEAMWORK The Ultimate Symbiotic Relationship Focusing on a common goal. Performing your job accurately so that the next person can do theirs. That's how we work together at ICON Clinical Research. Because at ICON, your personal best is the valuable link in the teamwork we need to achieve quality results.Working with ICON, you'll share in a unique culture of a large company that emphasizes a warm, friendly environment. This is where career possibilities can become realities... where those who look for challenges, embrace the learning and growth opportunities we offer.ICON Clinical Research is dedicated to providing the pharmaceutical and biotechnology industries with exceptional clinical research and biometrics services, and we're the first international CRO awarded ISO 9001:2000 quality certification across all divisions and functions.
Group Manager, Interactive Technologies
Raleigh, North CarolinaThe individual chosen for this position will manage all staff under his/her jurisdiction. Ensure that projects are conducted in a timely manner in adherence with ICON SOPs and appropriate regulations and to liaise with other department managers as necessary to achieve this. Additionally, you will monitor project budgets and communicate issues to department management in a timely manner. In this role, you will monitor the quality specification within projects/departments and liaise with clients on project related matters. You will ensure all necessary training is provided to his/her staff; Maintain documentation of training as appropriate and keep senior management informed of project status in relation to both quality and timelines. You will liaise with other managers/directors to improve the effectiveness of the organization. Maintain confidentiality of management information as appropriate and participate in business development activities as appropriate. Lastly, additional responsibilities may be assigned as required.The qualified candidate must have a background in medicine, science or other relevant discipline and appropriate experience. Experience/background in the clinical trial industry and specific IVR experience is preferred. The ability to coordinate all aspects of study management and to successfully manage project team(s) is a must. The selected individual must possess the ability to liaise successfully with clients. Foreign language skills are desirable. Current full driver’s license is required with the capability and willingness to travel at least 35% of the time (International and domestic: fly and drive).
Job Requirements
Come to ICON and be an important part of a well respected and growing company that believes the details of your career are every bit as critical as the work you do. You'll enjoy highly competitive benefits in addition to flexible scheduling, relocation assistance, tuition reimbursement, credit union, health club privileges, and many other exceptional advantages.TO APPLY and for more information on our opportunities and locations, please visit us at