Job Information
MMS Holdings Inc. Senior Manager, Medical Writing in Canton, Michigan
MMS is an award-winning, data-focused CRO that supports the pharmaceutical and biotech industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience and a data-driven approach to drug development make MMS a valuable CRO partner, creating compelling submissions that meet rigorous regulatory standards. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating and was named as the Best Global Biotech CRO in the 2018 International Life Sciences Awards. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn.
Roles & Responsibilities:
Provide leadership, mentor, and develop personnel by maintaining a positive work environment
Direct, manage and oversee the activities of direct reports
Responsible for development of colleagues
Provide training, feedback, direction and ensure quality of deliverable
Suggest and implement process improvements
Responsible for planning and resourcing for on-time delivery of project deliverables that meet quality objectives
Interact with clients on matters relating to contractual requirements, deliverable changes, timelines, and document content
Practice good internal and external customer service
Responsible for scientific medical writing and producing high quality documents
Demonstrate strong understanding of ICH guidelines, as applicable to medical writing
Create medical training exercises, train new medical writers, and serve as a mentor
Proficient with styles of writing for various document types
Interact directly and independently with clients to coordinate all facets of projects; competent communicator
Lead projects, including complex projects with multiple team members and independent coordination with client
Demonstrate excellent internal and external leadership skills for projects
Requirements:
College graduate in scientific, medical, clinical discipline or related field, or related experience
Has high level knowledge of drug development as it pertains to medical writing; has the ability to apply drug development knowledge during production of high quality documents
Experience with management in the pharmaceutical or CRO industry
Ability to anticipate and effectively resolve potential problems and client demands
Excellent scientific writing skills; willing to guide others in a variety of medical writing techniques
Proficiency with MS Office Applications
Excellent organizational and communication skills
Familiarity with ISO 9001:2008 requirements