Director, Regulatory and Medical Writing - Remote

Director, Regulatory and Medical Writing - Remote Join to apply for the

Director, Regulatory and Medical Writing - Remote

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DRM Arby's .About MMS : MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating. Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.We are looking for a motivated leader to join our Regulatory and Medical Writing Team!Responsibilities :

Oversees a team of Regulatory and Medical Writers, accountable for performance, team engagement, coaching, and mentorship.Considers impact intra- and extra-departmentally, responding accordingly (training, initiatives, tools, templates, etc.).Proficient with QC, MW tools, training, and processes; provides mentorship to others.Works on complex issues requiring in-depth knowledge of the company.Participates in corporate development of methods, techniques, and evaluation criteria for projects, programs, and people.Directs and controls activities of a broad functional area through several department managers.Oversees planning, staffing, and recommending and implementing changes to methods.Experienced in understanding the impact of updates in related deliverables; mentors others.Competent with managing client meetings and CRMs; provides mentorship to others.Proficient with managing projects from start to finish; considers impact to department and business needs.Identifies and mitigates project risk, including assessing client gaps.Adept at handling client feedback with appropriate follow-up or resolution.Provides strategic input in Resource Management related to potential areas of growth.Functions as a Business Lead, client-facing, promoting regulatory and medical writing service line.Requirements :

College graduate in Scientific, Medical, or Clinical discipline or related field, or related experience; Masters or PhD preferred.Minimum of 10 years’ experience in Regulatory or Medical Writing, or similar field required.Prior direct line management experience required.Ability to anticipate and effectively resolve potential problems with client demands.Demonstrates managerial skill and experience.Proficiency with MS Office applications.Hands-on experience with clinical trial and pharmaceutical development preferred.Good communication skills and willingness to work with others to clearly understand needs and solve problems.Excellent problem-solving skills.Good organizational and communication skills.Understanding of CROs and scientific and clinical data / terminology, and the drug development process.Seniority Level : DirectorEmployment Type : Full-timeJob Function : Health Care ProviderIndustries : Smart Meter Manufacturing

If you would like to know a bit more about this opportunity, or are considering applying, then please read the following job information.#J-18808-LjbffrRemote working / work at home options are available for this role.