University Of Michigan Work Values

Daily Duties at University Of Michigan:

UNIVERSITY OF MICHIGAN HOSPITAL – Ann Arbor, MI 2/1987-5/2004 Clinical Research Associate II (7/02-5/04) Skillfully managed multiple Phase I-III oncological clinical trials. Performed patient accrual, eligibility, and registration procedures. Wrote and distributed serious adverse event, data safety, and monitoring reports to medical personnel and external agencies. Collaborated with pharmaceutical companies to implement and complete studies. Processed monthly financial reports. Handled and shipped specimens. Ensured compliance with all GCP, ICH, IRB, and FDA regulations and guidelines, and prepared for QARC and other audits. Facilitated closeout meetings. Created presentations for SPORE meetings and conferences. Key Achievements: Displayed nursing expertise and a commitment to accuracy in the implementation of several concurrent studies. Ensured compliance with all GCP, , IRB, and FDA regulations and guidelines, and prepared for QARC and other audits.

What they like about University Of Michigan:

You give high priority to hiring firms with prestige. Market reputation and prestige of a firm may be determined through on-line research, and conversations with individuals working in your target industry. Note that firms "in the public eye" receive a great deal more critical publicity and attention than those operating with more anonymity. So as you assess your employment opportunities, be sure to seek out the positive aspects of the firm's reputation in addition to noting negative publicity the company may have received.

Tags

Registered Nurse, RN, Clinical Research, research, Boston, Michigan, CRO

Skills

Experience with backround managing multiple clinical trial studies including aspects of patient accrual and registration, adverse and serious event reportin and close out meetings, Coordination, presentation, and communication skills, with an ability to provide essential information to patients, medical professionals, and all levels of personnel., Commitment to team approach and building, loyalty and hard work, Experience in providing care and education to patients with diverse serious medical conditions, Microsoft Word, Excel, Power Point and Access, Able to perform Regulatory Process of a clinical trials from protocol application, consent writing and yearly continuation reports to the IRB and Closing the study., Compliance will GCP, IRB and FDA regulations

These are some of the questions we asked our climbers about their experiences with University Of Michigan: