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Primary Clinical Research in Omaha seeks a Clinical Research Coordinator to manage all aspects of assigned trials on-site. You will screen participants, recruit, schedule visits, and obtain informed consent in compliance with study protocols.
Daily tasks include collecting data, maintaining source documents, updating databases, and coordinating with investigators, sponsors, and CROs. Strong knowledge of GCP/ICH and regulatory standards is essential.
Primary Clinical Research in Omaha seeks a Clinical Research Coordinator to manage all aspects of assigned trials on-site. You will screen participants, recruit, schedule visits, and obtain informed consent in compliance with study protocols.
Daily tasks include collecting data, maintaining source documents, updating databases, and coordinating with investigators, sponsors, and CROs. Strong knowledge of GCP/ICH and regulatory standards is essential.