MMS Holdings Inc. is seeking an experienced Medical Writer to join our regulatory documentation team. You will ensure compliance with CFR Part 11, FDA, GCP; mentor junior staff; lead complex writing projects from start to finish.
The role requires a strong background in regulatory and medical writing, familiarity with ISO 9001/27001, and ability to manage client expectations and deliver high-quality submissions across clinical trial programs.
#J-18808-Ljbffr
Senior Medical Writing & Regulatory Manager in Manchester employer: MMS Holdings Inc
MMS Holdings Inc. is an exceptional employer that values innovation and excellence in the field of regulatory and medical writing. With a strong commitment to employee development, we offer comprehensive training programs and mentorship opportunities, fostering a collaborative work culture that encourages growth and creativity. Located in Greater London, our remote work flexibility allows you to balance your professional and personal life while contributing to impactful projects in a global environment.
