Proclinical - IT - Administration

Join our Boston team as a Veeva Clinical Business Administration Specialist. You will optimize Veeva Vault Clinical systems, providing crucial user support and driving process improvements. The role requires expertise in eTMF/CTMS, system validation, and clinical trial processes. This is a key op...

Lead document quality and submission readiness for a top pharmaceutical firm in Cambridge, US. Utilize your regulatory publishing expertise to manage and QC clinical documents like CSRs and IBs, ensuring eCTD compliance. This role demands sharp detail-orientation and proficiency in MS Office/Adob...