CSR Narrative Writing Consultant

Company: MMS
Location: Canton
Posted on: March 19, 2023

Job Description:

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. Strong industry experience, technology-enabled services, 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 the company has been recognized as a leading CRO in -Global Health & Pharma's -international awards programs for the last three consecutive years. For more information, visit or follow MMS on .This is a project-based consulting opportunity. -Roles and Responsibilities

• Responsible for writing safety documents intended for submission to regulatory agencies.
• Responsible for writing patient CSR narratives and producing high quality documents
• Practices excellent internal and external customer service
• Good understanding of MS Word for advanced writing techniques
• Address client comments during document lifecycle, manage revisions, and review deliverables with limited mentor oversight prior to releasing to client
• Ensure documents comply with appropriate ICH and regulatory guidelines
• Interact directly and independently with client
• Ability to follow MMS and sponsor processes
• Practices internal and external leadership skillsRequirements -
  • Over 3 years experience writing CSR narratives
  • College graduate in scientific, medical, clinical discipline or related field, or related experience
  • Prior medical/ narrative/ safety -writing experience preferred; Interested in expanding knowledge of drug development as it pertains to narrative writing
  • Master's or PhD in a scientific, medical, or clinical discipline preferred
  • 1-3 years' experience with regulated scientific/clinical or pharmaceutical, biotech or clinical research environment -
  • Understands ICH guidelines, as applicable to writing for clinical studies
  • Excellent written English skills
  • High degree of organization and able to manage multiple projects at any given time
  • Attention to detail and committed to excellence in all aspects of their work
  • Excellent communication and interpersonal skills
  • Proficient in Microsoft Word and Adobe Acrobat
  • Experience in the use of an Electronic Document Management systemPowered by JazzHR

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