"At ICON, it's our People that set us Apart"



ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development - from compound selection to Phase I - IV clinical studies.



ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.

You will effectively manage the activities of individual studies in a manner that ensures all timeframes and targets are met and that costs are kept under control.



Additional responsibilities include:



- With support, lead the development and maintenance of project management documents, including but not limited to, project timelines, project management plans, communication plans and risk analysis plans.

- With support, lead the review/approval of project related materials, including but not limited to, protocol/guidelines, informed consent forms, case report forms, site training materials, reports and newsletters.

- With support, monitor the quality specification within the project.

- Liaise with clients on project related matters.

- Lead the assessment of site training and management processes (with the Research Services Group) in an effort to ensure project efficiency and consistency.

- Lead the management of project financials, including but not limited to, change in scope, client and vendor invoicing/reimbursement and grant payments.

- Keep individual project costs under control.

- Minimum required education is a Bachelor's degree or equivalent (with a background in medicine, science or relevant discipline preferred).

- Two or more years of relevant experience are required (prefer clinical trials project management experience, Phase II / III).

- Proficient in computer applications such as Word, Excel, PowerPoint & Publisher.

- Excellent communication skills, both verbal and written.

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 compensation and an exceptional benefits package.



To apply directly, click on the following link (or paste into a browser) and search for Requisition #526: http://www.iconclinical.com/careers/job-opportunities/job-search/index.xml



ICON is an Equal Opportunity Employer committed to strength in diversity.