Participates in the design, administration and monitoring of clinical trials. Analyzes and evaluates clinical data gathered during research. Ensures compliance with protocol and overall clinical objectives. Knowledge of FDA regulatory requirements is required. May require ACRP or SOCRA Clinical Research Professional exam completion. Requires a bachelor's degree in Science or its equivalent. Typically reports to a supervisor or manager. Work is closely managed. Works on projects/matters of limited complexity in a support role. Typically requires 0-2 years of related experience.
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Company Description. Ergomed Group is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia. Our company allows for employee visibility (you have a voice. ) creative contribution and realistic career development. We have nourishe...
Company DescriptionAbout IDEXCEL, INCIdexcel is a global staffing and IT services organization, with a mission to bring great people and great organizations together. Our diverse client base represents a wide range of industries, including technology, telecom, insurance, healthcare, manufacturing, banking & financial services, food & commodities trading and federal organizations. Our teams of experienced recruiters directly work with client compa...
Job Description. When the work you do every single day has a crucial impact on the lives of others, every effort, every detail, and every second matters. This shared culture of happiness, passion, and dedication pulses through Cedars-Sinai. We invite you to consider this phenomenal opportunity. . As a Clinical Research Associate I, you will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Prin...
Location. Bethesda, MD 20817 US (Primary). Category. Clinical Operations. Job Type. Full-Time. Education. Bachelor's Degree. Travel. Up to 50%. Job Description. Provides site management and monitoring support for sponsored clinical studies. primarily Phase I and II, with limited Phase III and IV. Performs on-site pre-study/qualification, initiation, routine, and close-out visits. Prepare site visit reports and provide assistance to site staff in ...
Job Description. � Provides site management and monitoring support for sponsored clinical studies. primarily Phase I and II, with limited Phase III and IV. � Performs on-site pre-study/qualification, initiation, routine, and close-out visits. Prepare site visit reports and provide assistance to site staff in resolving deficiencies. � Educates and trains site and study staff in management of sponsored studies, including assurance to regulato...
Provide clinical and administrative support for the division of DEM (Diabetes, Endocrinology and Metabolism) in the areas of clinical research and regulatory compliance. Support administrator with the processing of all IRB and regulatory paperwork. Duties will also include working with current and potential research subjects
Requisition Details. GENERAL REQUISITION INFORMATION. EEO Statement. UNMC is an Affirmative Action Equal Employment Opportunity Employer, including an equal opportunity employer of protected veterans and individuals with disabilities. Location. Omaha, NE. Requisition Number. Staff_12954. Department. Neurological Sciences 50001975. Business Unit. College of Medicine. Reg-Temp. Full-Time Regular. Work Schedule. Monday - Friday. 8:00AM - 4:30PM. Rem...
