Job Details

Medical Writer Position

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.

Roles and Responsibilities:

1. Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias
2. Write and edit clinical development documents, including but not limited to, Informed Consent Forms and Clinical Protocols
3. Complete writing assignments in a timely manner
4. Maintain timelines and workflow of writing assignments
5. Practice good internal and external customer service
6. Highly proficient with styles of writing for various regulatory documents
7. Expert proficiency with client templates & style guides
8. Interact directly and independently with client to coordinate all facets of projects; competent communication skills for projects
9. Contribute substantially to, or manages, production of interpretive guides
10. Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary
11. Mentor medical writers and other members of the project team who are involved in the writing process

Requirements:

• At least 3 years of previous experience in the pharmaceutical industry
• Must have at least 3-5 years of industry regulatory writing and clinical medical writing experience
• The ideal candidate would hold a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline
• Oncology, General Medicines, Infectious Diseases and Vaccine experience preferred
• Substantial informed consent and clinical study protocol experience, as lead author, required
• Experience leading and managing teams while authoring regulatory documents with aggressive timelines
• Experienced in understanding complex clinical information
• Translate complex medical and scientific information into clear, patient-friendly, language
• Experienced in collaboration and cross-functional communication
• Exceptional writing skills are a must
• Excellent organizational skills and the ability to multi-task are essential prerequisites
• Candidate must be an expert in MS Word, Excel, PowerPoint, and related word processing tools
• Experience being a project lead, or managing a project team
• Strong understanding of federal regulations, Good Clinical Practices, and ICH guidelines a plus
• Not required, but experience with orphan drug designations and PSP/PIPs a plus