Clinical Research Coordinator

4 weeks ago


Santa Monica, California, United States Ampcus Full time
Job Title: Clinical Research Coordinator Job Summary: We are seeking a highly organized and detail-oriented Clinical Research Coordinator to join our team at Ampcus. The successful candidate will be responsible for the operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. Key Responsibilities: * Implement research activities for one or more studies, recognizing and performing necessary tasks to manage projects and prioritize work to meet necessary deadlines. * Plan and organize necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). * Collaborate with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support. Requirements: * Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience. * Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GCP) for clinical research. * Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships. * Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness. * Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment. * Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines. * Ability to respond to situations in an appropriate and professional manner. * Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines. * Ability to be flexible in handling work delegated by more than one individual. * Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications. * Ability to handle confidential material information with judgement and discretion. * Working knowledge of the clinical research regulatory framework and institutional requirements. * Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets. * Be available to work in more than one environment, travel to meetings, off-site visits, conferences, etc. What We Offer: * Competitive salary and benefits package. * Opportunities for professional growth and development. * Collaborative and dynamic work environment. * Recognition and rewards for outstanding performance.

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