Proclinical is seeking an Associate Director of Regulatory Affairs to lead global regulatory strategy and submissions for oncology development programs on a worldwide scale. This remote, contract-based role requires strong leadership in cross-functional planning and risk mitigation.
You will act as Global Regulatory Lead across development programs, aligning strategies with clinical, nonclinical, and CMC plans, and guiding health authority engagement, including designation applications like
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Global Regulatory Lead, Oncology – Remote 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.
