Clinical Data Manager, PS # 293332

We work together to find a better way and break new ground to make progress possible. Focused on common goals, we raise the standard and make a difference. We strive for excellence in everything we do. At ICON, career possibilities can become realities for those who look for challenges and embrace learning and growth opportunities. ICON Clinical Research is dedicated to providing the pharmaceutical and biotechnology industries with exceptional clinical research and biometrics services. Join us in one of our current openings and enjoy highly competitive benefits and exceptional advantages. CLINICAL DATA MANAGER Data Management USA Redwood City, CA EXEMPT POSITION: The successful candidate will effectively manage the clinical data function under the general direction of the VP of Data Management USA. Will manage Clinical Data Management staff in a manner that ensures all timeframes and targets are met with the highest quality to the sponsor’s satisfaction, and that costs are kept under control. Will be responsible for hiring, training, and maintaining the appropriate staff for projects. Will also be responsible for planning, implementing and delivering the data management projects in accordance with the contracts agreed with the sponsors, managing projects in a timely manner in adherence with ICON SOPs and appropriate regulations, and to liaise with other departments and Project Managers as necessary. Will also provide business development support by assisting with the preparation of bids, making presentations to clients and bid defenses. Prepare and manage the overall projects' budgets through out the life cycle of the project, and takes overall responsibility for cost control, timelines and project quality keeping senior management informed of all appropriate issues. REQUIREMENTS: The qualified candidate will have a B.S. degree or equivalent experience in a medical background, with at least 5 years of clinical data management experience and one year of supervisory experience, including project managemetn, resource planning, staff recruitmetn, performance evaluations, career development and training. Knowledge of FDA regulations respecting data quality and clinical trials conduct. Knowledge clinical databases,i.e. Medidata and Phase Forward. Strong written and oral communication skills. Proven leadership skills. Ability to work within a team environment. Ability to manage competing priorities in a changeable environment. Ability to handle stressful situations and deadlines. Excellent interpersonal skills. TO APPLY and for more information on our opportunities and locations, please visit us at www.iconclinical.com and click on EMPLOYMENT OPPORTUNITIES.http://www.iconclinical.com/index.asp?getpage=true&sid=10 No agencies, please. 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 www.iconclinical.com No agencies, please. ICON. A Symbol of Excellence. ICON Clinical Research is an Equal Opportunity Employer committed to strength in diversity. www.iconclinical.com To Apply for this position, please CLICK HERE