IQVIA in Mexico City seeks a Clinical Study Report (CSR) Document Specialist responsible for populating, tracking, and performing quality checks on CSR appendices. Candidates should have a Bachelor's degree in life sciences or related fields, fluency in English, and 1 to 2 years of eTMF experience. This role requires effective communication, attention to detail, and the ability to work collaboratively in a fast-paced environment. Join a diverse team committed to quality in clinical documentation.
#J-18808-Ljbffr