Participates in the design, administration, and execution of clinical research trials. Conducts standard tests in accordance with established policies and procedures. Analyzes and evaluates clinical data gathered during research. Ensures compliance with protocol and overall clinical objectives. Possesses knowledge of FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and JCAHO and International Conference on Harmonization (ICH) guidelines. Requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. Work is closely managed. W ...orks on projects/matters of limited complexity in a support role. Typically requires 0-2 years of related experience.More Show Less
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Job Title: Clinical Research Associate I. Location: Durham, NC. Hours/Schedule:8 hours per day, 40 hours per week - Flexible day shift - 3 days on site weekly. Type: Contract. Job Description. The manager would be looking for this person to work in the office 3 days a week. This is considered a level 1 position (slightly above entry) as they will need to have experience with onsite monitoring. JOB DESCRIPTION. Assists in the management of the cli...
Job Description. Job Description. POSITION TITLE. Clinical Research Associate I. DEPARTMENT. Monitoring. Ora Values the Daily Practice of …. Prioritizing Kindness. Operational Excellence. Cultivating Joy. Scientific Rigor. At Ora, we are building the future of ophthalmic clinical research. As the world's leading full-service ophthalmic drug and device development firm, we guide our clients across all phases of clinical research to efficiently bri...
