Job Details

Provides centralized, non-site-facing support to CRAs and clinical project teams across the study lifecycle.Supports consistent site oversight by maintaining study documentation and systems.Works in close collaboration with assigned CRAs and under the oversight of the CTM.Essential Functions:Prepare and maintain Investigator Site Files, including document distribution and coordination.Review eTMF for completeness and identify documents requiring follow-up.Perform scheduled reconciliations between Delegation of Authority Log, CTMS, eTMF, and system-access records.Qualifications:Bachelor's degree in a scientific, healthcare, or related discipline.Initial experience in clinical research, clinical trial administration or study coordination within a CRO, pharmaceutical, or biotech environment.Practical experience using CTMS, eTMF, and other clinical trial systems.Skills and Competencies:Strong organization, prioritization, and follow-through across multiple studies and deadlines.High attention to detail and ability to perform accurate document and data review.Ability to work independently in a remote environment while collaborating effectively with CRAs and CTMs.Precision for Medicine Precision for Medicine is a clinical research organization specializing in oncology and rare disease. The company prides itself on a strong culture with high employee retention rates.#J-18808-Ljbffr