Develop Clinical Investigation Plans (CIPs), Informed Consent Forms (ICFs), Study Management Plans, Case Report Forms (CRFs), and support the creation and maintenance of full clinical study documentation. * Provide support for internal or external audits/inspections and ensure resolution of audit/inspection findings related to assigned clinical projects. * Conduct site management & monitoring, clinical product management, and clinical field support activities/visits, as needed. * Conduct, attend, or support training and observational activities, as needed, for study team members. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
mehr