A multi-lateral, collaborative partnership of hospitals and institutions in Thailand, United Kingdom, United States, and Vietnam is looking for a Senior Training Officer with extensive experience in clinical trials management and the training requirements for research sites to be prepared conduct such trials. Knowledge of and experience in training areas include topics related to conducting clinical research, such as ICH-GCP, protocol specific training, IRB responsibilities, human subjects protection and research ethics, study/project management, safety reporting is required.
Essential Criteria: · Ability to develop training agendas and instructional material using a range of media. · Hands-on experience conducting and leading training sessions of groups of various sizes. · Experience evaluating the success and impact of training on the target audience. · Working knowledge of clinical trials operations through work experience as well as academic knowledge. · Demonstrate knowledge and support of the principles, details, and application of the ICH Good Clinical Practices (GCP). Desirable Criteria: · High level of organizational and record keeping skills. · Excellent spoken and written English. · Excellent interpersonal skills with ability to communicate clearly and effectively at all levels. · Demonstrated experience using Microsoft Office (Word, Outlook, Excel, PowerPoint). Experience with MS Project a plus. · Ability to communicate clearly and professionally through email, conference calls, and in face-to-face contacts and meetings. · Requires creative flexibility to react quickly to unexpected problems with training venues and problems with equipment availability. Completed applications (CV and Cover Letter) should be sent to the Administrator, Eijkman-Oxford Clinical Research Unit, Lembaga Biologi Molekuler Eijkman, Jl. Diponegoro 69, Jakarta 10430 or e-mail to: [EMAIL PROTECTED] org. Please quote the reference "Training Officer". The closing date for applications is 8 August 2008.
