Date Posted [Jun-24-09] (ID: 81312)
ICON Clinical Research has an immediate opportunity for an
Associate Director, Phase IV in our Lifecycle Sciences Group. You will effectively manage the activities of project managers and staff in a manner that ensures all timeframes and targets are met and that costs are kept under control. In addition, you will serve as a senior level liaison with clients as appropriate, represent LSG in business activities, provide leadership and assist as appropriate in managing PM department of LSG in an effective manner. Responsibilities include, but are not limited to:
• Manage projects in a timely manner in adherence with SOPs and appropriate regulations and work with other department managers as necessary to achieve this.
• Provide senior oversight to the development and maintenance of project management documents, including but not limited to, project timelines, project management plans, communication plans and risk analysis plans.
• Provide senior oversight to 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.
• Work with clients on project related matters.
• Provide senior oversight to the assessment of site training and management processes in an effort to ensure project efficiency and consistency.
• Provide senior oversight to 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.
• Keep senior management informed of project status in relation to quality, timelines and staff issues.
• Lead participation in the interviewing process and hiring efforts.
Position Qualifications and Required Experience: • Minimum required education is a Master’s degree or equivalent, with a background in medicine, science or relevant discipline preferred.
• Six or more years of relevant experience required.
• Significant expertise in Phase IV studies, from study design and development to project management.
• Demonstrated resourcefulness and promotion of the development of new ideas and solutions.
• Ability to adapt to changes in deadlines and changes in nature of assignments.
• Proficient in computer applications such as Word, Excel, PowerPoint, and Publisher.
• Ability to travel (International and Domestic) up to 35%.
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 that includes: Medical, Dental, and Vision Insurance, Flexible Spending Accounts, Short Term and Long Term Disability, Life and AD&D Insurance, 401K Plan with matching contributions, a generous program of Vacation, Holidays and Personal Time Off and more.
ICON. A Symbol of Excellence.
ICON Clinical Research is an Equal Opportunity Employer committed to strength in diversity.
www.iconplc.comJob Title - Associate Director, Phase IV - Registry - Observational Study
Company Name - ICON Clinical Research
Email - william.vannewkirk@iconplc.com
Website- http://www.iconplc.com