Proclinical seeks an Aggregate Reports Specialist to lead PV activities across drug safety programs in a remote role. You will coordinate aggregate reports, PSURs/DSURs, line listings, and RMP-related tasks, ensuring timely, compliant outputs with CRO and global teams.
The role requires strong data analysis, regulatory knowledge, and collaboration with safety physicians and study teams to drive continuous process improvement in signaling and risk management.
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Remote Aggregate Safety Reports Specialist in Cambridge employer: ProClinical
Join a globally recognised biopharmaceutical organisation that prioritises innovation and collaboration in the field of protein science and biologic drug development. With a strong commitment to employee growth, you will have access to continuous learning opportunities and be part of a supportive team dedicated to delivering life-changing therapies. Located in a vibrant area, this role not only offers meaningful work but also a dynamic work culture that values your contributions and fosters professional development.
