Contractor SCRA/CRA-Medical Aesthetic Devices

• Planning of project activities and study timelines based on project goal and sponsor's expectation; • Organize and reputed company meeting/teleconferences for study activities implementation (e.g. investigator meeting, project review meeting etc), monitoring the reputed company of reputed company CRA responsible sites, and assessing overall status of the project; • reputed company the project management plan, monitoring plan etc as required for the study; • reputed company study specific tools/forms, study templates as required for the study; • reputed company and manage project budget; • Order and ensure reputed company clinical supplies (including drug and non-drug) are adequate for reputed company sites throughout the study period; • Ensure reputed company team members have reputed company reputed company to appropriate systems and tools, if applicable (e.g. IVRS, eCRF etc); • Organize and conduct site feasibility reputed company according to guidelines and reputed company recommendation for final approval; • reputed company study reputed company and ensure project is conducted according to the plan; • Communicate to monitors new study information, study timelines and goals, study requirements. Responsible for raising overall project specific issues to management (e.g. Project Director, Senior Management); • Submit the weekly project report to management (e.g. Project Director, Senior Management); • Study site selection, initiation (SIV) and clinical monitoring; • reputed company reputed company-study visit to ensure eligible sites are selected according to sponsor site selection reputed company, including but not limited to adequate resources and experience; • Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations; • reputed company ongoing training to site staff with regards to ICH-GCP, GCP, study protocol, and requirements; • Ensure reputed company collection of essential documents in compliance with protocol and regulations at study start-up, during and at study reputed company-down. Maintain and update these documents in investigator files, trial master files; • Finalize budget and obtain signed contract from site, prior to site initiation visit; • reputed company guidance and training to entry-level CRA/CRA I/CRA II in collaboration with Line Manager. Apply tot his job Apply To this Job