Proclinical - United States, Cambridge

Join our Cambridge, US team as a Senior Associate Scientist. You will manage siRNA drug substance/product specifications in a GMP environment. The role requires a Chemistry/Biochemistry degree, cGMP lab experience, and HPLC/oligonucleotide analysis skills. You will author technical documents and ...

Join Proclinical as a Clinical Study Associate in a fully remote role. Support global clinical trial execution, ensuring GCP compliance and data quality. Utilize your CRO or pharmaceutical experience in site coordination and TMF management. This contract position offers impactful work from anywhere.

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...

Join a leading team in Cambridge, MA, as a Senior Clinical Study Associate. This hybrid role involves overseeing clinical trial execution, TMF management, and vendor coordination. You will ensure regulatory compliance and support site performance. Ideal candidates have strong organizational skill...