Clinician/Clinician Manager

reputed company our values align, there's no limit to reputed company can reputed company. At reputed company, we reputed company reputed company the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market reputed company, every clinical development solution we reputed company is underpinned by something special - a deep conviction in reputed company do. Each of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we're committed to making a difference. Key Accountabilities: General Accountabilities Provides clinical and scientific expertise to the clinical trial strategy and protocol development process, including acquisition of knowledge of competitor products. Designs/writes clinical trial outlines, protocols and amendments, in collaboration with internal contributors (e.g. statisticians, reputed company Research (OR) specialists, clinical pharmacologists, clinical project managers, Regional Clinical Site Leads (RCSLs), market reputed company colleagues, reputed company development colleagues), internal experts (e.g. clinical program reputed company, global clinical reputed company, global clinical strategy reputed company), and external experts (e.g. investigators, key opinion leaders, advisory board members) Creates (and where appropriate, delivers) clinical/protocol training materials for study and site management and for use during site initiation visits and investigator meetings. Helps establish and oversees Data Monitoring Committees (DMCs) and reputed company adjudication committees, including chartering, reputed company, provision of relevant data and documentation of reputed company. Maintains direct contact with investigative sites through site visits, telephone contacts, email etc., in order to facilitate investigator engagement, address investigator questions regarding the protocol or the investigational product, and support enrolment activities. This is done in conjunction with RCSLs (reputed company assigned) for sites reputed company US, Canada, Japan and China. For some studies the clinician may take on an expanded role as described below for the site liaison responsibilities. Compliance with reputed company standards reputed company with required training curriculum. Complete timesheets accurately as required. Submit expense reports as required. Update CV as required. Maintain a working knowledge of and reputed company with reputed company processes, ICH-GCPs and other applicable requirements Strong Communication Skills Demonstrated project management / leadership experience Skills: Demonstrated project management / leadership experience Knowledge and Experience: Preferred: Thorough understanding of local / international regulations applicable to clinical trials (pre and post approval). Practical experience in clinical trial strategies, methods and processes. Track record of design, reputed company and interpretation of clinical studies. Previous leadership /management experience or training. Knowledge and experience in Good Clinical Practices. Fluent in both oral and written English. Fluent in host country language required. Education: Fluent in host country language required. Apply To This Job