- IQVIA (Greenville, NC)
- …Req * Requires 10 years clinical research experience including 6 years of project management experience or equivalent combination of education, training and ... agreed upon approach. * Develop and/or support on the preparation of integrated study management plans in collaboration with the core project team. * Accountable… more
- ThermoFisher Scientific (Greenville, NC)
- …ensuring effective communication and addressing customer concerns. + Maintain project management documentation, including plans, timelines, and progress ... biotechnology field + Solid knowledge of drug development, clinical trial management , and/or GCP compliance processes +...software programs such as Microsoft Office for general use, project management , and presentations + Valid driver's… more
- ThermoFisher Scientific (Greenville, NC)
- …SOPs and regulatory requirements. The CTM is assigned a subset of clinical trial management responsibilities under the guidance and supervision of a CTL/CTM ... Trial Team (CTT) for trials with lower complexity in partnership with the Lead Trial Physician. The CTM manages operational planning, global coordination, and… more
- ThermoFisher Scientific (Greenville, NC)
- …moderate to high complexity, in compliance with ICH GCP. In accordance to project specific requirements, may assume Lead CTM responsibilities on regional level, ... responsibilities; eg process improvements, manage sophisticated programs, have wider management or project coordination responsibilities. + Develops clinical… more
- ThermoFisher Scientific (Greenville, NC)
- …responsibilities; eg process improvements, lead complex programs, have wider management or project coordination responsibilities. + Develops clinical tools ... solutions and deliver results; coordinating the activities of Clinical Management members which are allocated to a project...complexity, in compliance with ICH GCP. In accordance to project specific requirements, may assume Lead CTM… more
- ThermoFisher Scientific (Greenville, NC)
- …equipment, biocompatibility (ISO 10993), risk assessment and usability. + Demonstrated project management and communication (written and oral) skills to ... Office **Job Description** Join Thermo Fisher Scientific Inc. as a Clinical Trial Reg Affairs Manager specializing in medical devices and diagnostics and make… more