Proclinical - United States, IT - Administration

Proclinical is hiring a QA Document Control Associate in Rockville, MD to ensure GMP compliance through precise document lifecycle management. You will maintain electronic and hardcopy records, utilize Veeva, and support audits within the QMS. Ideal candidates have experience in Quality Systems D...

Join our team as an EHS Project Manager in Lexington, MA. You will develop and implement critical safety programs for facilities and construction projects within biotech/pharma. This role requires strong EHS regulatory knowledge and experience with risk assessment and management systems. We seek ...

Lead the development of Companion Diagnostics (CDx) from concept to care as a Project Manager in Tucson. You will create integrated plans, manage budgets, and mitigate risks to drive project execution. This role requires strong PM expertise to guide cross-functional teams and ensure quality throu...

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...