Medical Writer

Medical Writing and Regulatory Submissions Location : London (Hybrid, 4 days onsite) Type : Permanent, Full-Time Take your expertise in medical writing and regulatory submissions to the next level. We're seeking a team-oriented leader to oversee medical writing and regulatory processes, mentor team members, and ensure alignment with industry standards and organizational goals. This is a perfect role for someone ready to lead while remaining hands-on with complex projects. Responsibilities : Manage the preparation of clinical trial submissions and related documents. Mentor and train junior staff to build team expertise. Collaborate with internal and external stakeholders to ensure regulatory compliance. Regularly update Standard Operating Procedures (SOPs) and process maps. Qualifications : Proven experience in medical writing or regulatory affairs, with 3 years in a leadership capacity. Strong scientific writing and data interpretation skills. Advanced knowledge of regulatory frameworks and clinical trials. Join a collaborative team and contribute to the success of life-changing clinical trials. Please get in touch or email nfordycebarringtonjames.com

Location: London, GB

Posted Date: 1/15/2025