IQVIA Argentina is looking for a Clinical Study Report Document Specialist in Mexico City. This role involves leading the kick-off meetings for CSR appendices, ensuring compliance with regulatory standards, and managing document activities from authoring to finalization. The ideal candidate has a Bachelor's degree in life sciences or a related field, with 1-2 years of experience in eTMF and familiarity with document management systems. Attention to detail, independent working, and effective communication are crucial for success in this fast-paced environment.#J-18808-Ljbffr
Csr Document Specialist: Clinical Appendices & Qc Lead
IQVIA ARGENTINA
distrito federal, distrito federal
Publicado hace 20 días
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