Contractor SCRA/CRA-Medical Aesthetic Devices

Remote Worldwide Hiring now

• 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 each 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 timely reputed company to appropriate systems and tools, if applicable (e.g. IVRS, eCRF etc);
Organize and conduct site feasibility visits according to guidelines and reputed company recommendation for final approval;
Track 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);

Project Director, Senior Management);

Study site selection, initiation (SIV) and clinical monitoring;
reputed company pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, 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 timely 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

Apply for this role Takes you straight to the employer's application page — free, and no WFHNet account required.

More roles on the wire