Tigermed | Senior Clinical Research Associate (Western ...

1. Job Purpose:This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical study studies in accordance with Tigermed or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (ICH-GCP), Clinical Practice standard (GCP) and other applicable regulations;The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget.2. Responsibilities:Planning of project activities and study timelines based on project goal and sponsor's expectation;Organize and Lead meetingteleconferences for study activities implementation (e.g. investigator meeting, project review meeting etc), monitoring the progress of each CRA responsible sites, and assessing overall status of the project;Develop the project management plan, monitoring plan etc as required for the study;Develop study specific toolsforms, study templates as required for the study;Develop and manage project budget;Order and ensure all clinical supplies (including drug and non-drug) are adequate for all sites throughout the study period;Ensure all team members have timely access to appropriate systems and tools, if applicable (e.g. IVRS, eCRF etc);Organize and conduct site feasibility visits according to guidelines and make recommendation for final approval;Track study progress 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;Perform 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;Provide 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 close-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;Provide guidance and training to entry-level CRACRA ICRA II in collaboration with Line Manager.3. Qualifications:Bachelor degree or above in Medical, Pharmacology or Biology related major;Good understanding and knowledge of Good Clinical Practice and clinical trial operation processesprocedures;At least 1-3 years of CRA experiences;Good command of written and verbal English;Good skills on Microsoft Word, Excel, PPT and Outlook, etc.;Other abilities such as Communication skillsInformation-gathering skills. Knowledge andor experience in medical practice is a plus.Welcome passion and creative ideas' friends! Look forward to receiving your profiles.

Created: 2025-01-02