Senior Medical Writer (Remote) Job at MMS, Nashville, TN

QnRRa3RBZTgwY2RMdUhPVzlSMjVHRHZoR2c9PQ==
  • MMS
  • Nashville, TN

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 LinkedIn .

Responsibilities

  • 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
  • Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals
  • Complete writing assignments in a timely manner
  • Maintain timelines and workflow of writing assignments
  • Practice good internal and external customer service
  • Highly proficient with styles of writing for various regulatory documents
  • Expert proficiency with client templates & style guides
  • Interact directly and independently with client to coordinate all facets of projects; competent communicator skills for projects
  • Contribute substantially to, or manages, production of interpretive guides
  • Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary
  • 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
  • Substantial clinical study protocol experience, as lead author, required
  • Experience leading and managing teams while authoring regulatory documents with aggressive timelines
  • Experience in regulatory submissions (clinical study reports) presented to regulatory authorities a plus
  • Understanding of clinical data
  • 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
  • Substantial clinical study protocol experience, as lead author, required
  • Experience leading and managing teams while authoring regulatory documents with aggressive timelines
  • Not required, but experience with orphan drug designations and PSP/PIPs a plus

Job Tags

Remote job, Full time,

Similar Jobs

Ed Martin Toyota

Automotive Service Technician Job at Ed Martin Toyota

Service TechnicianMinimum 2 years experienceMinimum of 2 ASE certifications requiredTOP PAY FOR TOP TECHNICIANS"You can see photos of our shop and videos from our team about being an tech at Ed Martin on our WrenchWay Page: Every employee with Ed Martin Automotive...

Abacus Corporation

Forklift Operator Job at Abacus Corporation

 ...Abacus Staffing is seeking skilled and safety-conscious Forklift Operators to join our dynamic team. The ideal candidate will be responsible...  ...equipment to ensure efficient movement of goods within the warehouse. This role is essential in maintaining smooth operations in... 

Get It - Real Estate

Junior Mortgage Loan Officer - Remote | WFH Job at Get It - Real Estate

 ...eager to build a rewarding career in the mortgage industry? Do you thrive in a fast-paced...  ...seeking enthusiastic and driven Junior Loan Officers to join our growing team. This is your chance...  ...who is driven to perform at a high level. Technical Skills: Proficient with Microsoft... 

Applied Materials

Export Compliance Professional - Global Trade Compliance Job at Applied Materials

 ...supportive leading global company. Visit our Careers website to learn more about careers at Applied.**Export Compliance Professional - Trade Compliance****Overview** **:**It is an exciting time in the semiconductor industry and Global Trade compliance plays a critical... 

U.S. Silica Company

Operator Job at U.S. Silica Company

 ...company and is a leading producer of commercial silica used in the oil and gas industry and in a wide range of industrial applications...  ..., vendors, truck drivers and site visitors Education, Experience, Knowledge, Skills & Abilities: High School Diploma or GED...