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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Regulatory & Medical Writing Lead – Global Impact employer: MMS
At MMS, we are dedicated to creating a workplace where your expertise as a Principal Biostatistician is valued and nurtured. Our award-winning culture promotes collaboration and innovation, ensuring that you have the support and resources needed to excel in your role while contributing to meaningful projects in the clinical research field. With a strong focus on employee growth and a commitment to maintaining an inclusive environment, MMS stands out as an exceptional employer in the UK.
