Logo for Merit Medical Systems, Inc.

Senior Medical Writer

Key Facts

Remote From: 
Full time
Senior (5-10 years)
English

Other Skills

  • Internet Research
  • Word Processing
  • Mentorship
  • Microsoft Excel
  • Training And Development
  • Editing
  • Non-Verbal Communication
  • Time Management
  • Detail Oriented
  • Self-Motivation

Roles & Responsibilities

  • Bachelor’s degree in medical, biological, physical or engineering disciplines with at least five years of medical writing experience, preferably with Clinical Evaluation Reports (CERs).
  • Extensive knowledge of regulatory requirements for Clinical Evaluation Reports, including familiarity with FDA regulations, EU MDR (2017/745) and ISO 13485.
  • Proficient in searching medical literature and databases for clinical and technical information, with the ability to read, analyze and interpret regulations and complex documents.
  • Demonstrated supervisory experience and strong project management skills, plus excellent written and verbal communication.

Requirements:

  • Independently researches, prepares, writes, edits and reviews clinical evidence documents, such as CERs and SSCPs.
  • Supports regulatory approval processes by formulating clinical evidence documents and responding to regulatory agency questions.
  • Manages and maintains procedures, systems and processes to meet regulatory requirements for clinical evidence documents, ensuring up-to-date guidance and regulatory feedback.
  • Collaborates with cross-functional teams to ensure high quality work and successful project delivery.

Job description

Work Shift:

DAY

Work Schedule:

Why Merit?

At Merit Medical, our mission is to create innovative medical devices that improve lives. Our goal is to hire and develop people who want to build something special through hard work, team effort, and commitment. Together, we are making a difference in the lives of patients around the world.

ESSENTIAL FUNCTIONS PERFORMED

1.    Independently researches, prepares, writes, edits and reviews clinical evidence documents, e.g. CERs and SSCPs. 
2.    Conducts proofreading, editing, document formatting, review comment integration and document completion/approval activities.
3.    Supports regulatory approval process through clinical evidence document formulation and responding to regulatory agency questions.
4.    Manages and maintains the procedures, systems and processes required to meet regulatory requirements for clinical evidence documents and ensures they stay up-to-date based on guidance, regulation and feedback from regulators.
5.    Collaborates with cross-functional teams to ensure high quality and successful project delivery.
6.    Develops and maintains in-depth therapeutic and product operation knowledge; applies this knowledge to the development of well written clinical evidence documents.
7.    Provides input to post-market surveillance and risk management activities.
8.    Creates and manages schedule of deliverables.  
9.    Conducts training for medical writers, regulatory affairs and other functions, as needed.
10.    May supervise or mentor other medical writers, as assigned.
11.    Performs other duties and tasks, as required.

ESSENTIAL PHYSICAL/ENVIRONMENTAL DEMANDS 

•    Lifting -- Not to exceed 50 lbs. – local practice may apply.
•    Writing
•    Sitting
•    Standing
•    Bending
•    Visual acuity
•    Color perception
•    Depth perception
•    Reading
•    Field of vision/peripheral 

SUMMARY OF MINIMUM QUALIFICATIONS

•    Education and/or experience equivalent to a Bachelor’s Degree in the medical, biological, physical or engineering disciplines and five years of medical writing experience, preferably with CERs. 
•    Extensive knowledge of regulatory requirements relative to Clinical Evaluation Reports.
•    Proficient in searching medical literature and databases for clinical and technical information.
•    Ability to read, analyze, and interpret regulations, technical standards, guidance documents, test reports, clinical and medical terminology, technical product information and complex documents.
•    Knowledge of U.S. FDA regulations, the Medical Devices Directive (93/42/EEC, as amended), EU Medical Device Regulation (2017/745) and ISO 13485 Quality System Standards.
•    Effective written and verbal communication skills in the area of technical/clinical applications.
•    Supervisory experience.
•    Strong command of medical and surgical terminology.
•    Working knowledge of statistics.
•    Self-motivated, self-directing, strong attention to detail and excellent time management skills.
•    Project management skills.
•    Demonstrated computer skills preferably spreadsheets, word processing, internet research and other applicable software programs.

COMPETENCIES

•    Medical/technical writing skills
•    CER protocol and report development/writing
•    Medical literature research skills
•    Computer skills
•    Interpersonal/verbal/written communication skills
•    Project management skills
•    Statistical knowledge/application

COMMENTS

Infectious Control Risk Category III:

The risk category explains whether or not employees are likely to come into contact with blood or body fluids while performing their jobs.  Risk category III states employment and procedures that do not require exposure.

As an eligible Merit employee, you can expect the following:

* Multiple Shifts and Hours to choose from: Days, Swing (Eve), and Nights

* Medical/Dental & Other Insurances (eligible the first of month after 30 days)

* Low Cost Onsite Medical Clinic

* Two (2) Onsite Cafeterias

* Employee Garden | Gardening Classes

* 3 Weeks' Vacation | 1 Week Sick-Time | Paid Holidays

* 401K | Health Savings Account

To see more on our culture, go to www.merit.com/careers.

Military Veterans are encouraged to Apply.

Merit is a proud Utah Patriot Partner committed to hiring our Veterans.

Medical Writer Related jobs

Other jobs at Merit Medical Systems, Inc.

We help you get seen. Not ignored.

We help you get seen faster — by the right people.

🚀

Auto-Apply

We apply for you — automatically and instantly.

Save time, skip forms, and stay on top of every opportunity. Because you can't get seen if you're not in the race.

AI Match Feedback

Know your real match before you apply.

Get a detailed AI assessment of your profile against each job posting. Because getting seen starts with passing the filters.

Upgrade to Premium. Apply smarter and get noticed.

Upgrade to Premium

Join thousands of professionals who got noticed and hired faster.