Clinical Project Manager - Devices

Aspire to set new standards for excellence. A global specialty pharmaceutical and medication delivery company, Hospira is Advancing WellnessTM by discovering, developing, manufacturing, and marketing high-quality hospital products and technology solutions. We’re among the leaders in our field, backed by decades of experience. We use unique methods to create dramatic results and we empower each employee to explore new ways of improving the safety and effectiveness of patient care – with integrity, speed, and a sense of personal accountability to patients around the world.As a leader and an innovator, we take great care to hire, develop, and keep the right people – people of integrity who are motivated by challenges, take ownership of their careers, embody our values and embrace entrepreneurial spirit. Clinical Project Manager - Devices In this role you will oversee project management of all device clinical studies, customer preference studies and device development site partnership studies, along with personnel development, mentoring of clinical research associates and other clinical staff. This will include overall management of clinical research organizations and vendors. Primarily you will supervise the development and execution of clinical studies, customer preference studies and development site partnership studies, for all device projects. You will also be responsible for medical device development study documentation including human factors usability study protocols and SOP’s. Additionally, you will plan and coordinate Scientific Advisory Board (SAB) meetings related to device development projects.To be successful in this position, you must possess: Bachelor’s degree is required, preferable in a Science or health related field; Post-graduate training in a health related field or equivalent experience is desirable Minimum of 3+ years experience as a Clinical Project Manager or 7+ years experience in Clinical Research is preferred 2-5 years of prior budget/project management experience is preferred In-depth knowledge of FDA, International Council on Harmonization and local regulations as they apply to clinical research Working knowledge and experience with device development activities is required, along with familiarity with Scientific Advisory Board planning Effective scientific writing and professional presentation skills Excellent oral and written communication skills are required Strong ability to interface with internal and external customers Capability to work independently while functioning as part of an integrated teamHospira offers an agile, yet balanced work culture and the types of compensation and benefits you’d expect from an industry leader. We provide the tools and resources you need to reach and exceed your career goals through professional development, education reimbursement, and much more.To what do you aspire? Learn more about us and apply online: https://sjobs.brassring.com/1033/ASP/TG/cim_jobdetail.asp?jobId=139424&type=search&JobReqLang=1&recordstart=1&JobSiteId=5100&JobSiteInfo=139424_5100&partnerid=16015&siteid=5100 Req #: 5007BRAs an equal opportunity/affirmative action employer, Hospira embraces diversity of thought and cultural perspective and fosters an environment of empowerment, fairness and respect.