Regulatory & Medical Writing Lead – Global Impact

MMS, a data-focused clinical research organization, invites you to join a collaborative, innovative team in Belfast. The role focuses on regulatory and medical writing leadership, mentoring others, and guiding complex trial documentation and regulatory submissions.

With extensive experience in CRO environments, you will oversee projects from start to finish, manage client meetings, and drive high-quality deliverables while mitigating risks and ensuring compliance with ISO, FDA, and GCP

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