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Medical Writer, GBS Job in Bogotá Recruiting by Zimmer Biomet

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Medical Writer, GBS

🏢 Zimmer Biomet
📌 Bogotá, Bogota, Colombia
💼 arts design entertainment sports and media
⌚ 8 hours ago

🔖 Full Time

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At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance We are committed to creating an environment where every team member feels included, respected, empowered, and

What You Can Expect

The Medical Writer is primarily responsible for preparing Clinical Evaluation Reports (CERs) for regulatory submissions and Post-market Surveillance Plan literature reviews (PSPs) for analysis of existing product clinical Both involve conducting searches of peer-reviewed publications, national implant registries, risk management files and post market quality tabulations to compile relevant Report preparation involves summarizing data found and drafting risk versus benefit analyses for review by Senior Medical Writer or The scope includes products of Reconstruction, Trauma, Biologics or other ZB Divisions as

How You'll Create Impact

Identify pertinent internal and external sources of clinical data and conduct systematic literature searches of peer review
Prepare Clinical Evaluation documents according to the applicable regulations (including MDR (EU) 2017/745) and Zimmer Biomet internal procedures using relevant information compiled from clinical research, peer reviewed publications, risk management files and post market
Summarize findings and draft risk versus benefit analyses and conclusions, for review by Medical Writing Manager or designee, based on clinical and post market
Distribute reviewed final draft reports to Clinical Affairs, Regulatory Affairs, Post-Market Surveillance and Development Engineering groups to verify and approve content of final draft
Prepare reviews of peer-reviewed literature for inclusion in Zimmer Biomet post-market surveillance (PMS)
Support the Manager or Team Leader for Audit activities including the participation in Audits as clinical evidence SME as needed
File work in the Clinical Evaluation archives, provide clinical data searches and documentation as a service to various functions within Zimmer Biomet, and provide verbal and/or written progress reports

What Makes You Stand Out

Demonstrated technical and medical writing competence
Strong organizational skills, attention to detail and proofreading skills
Understanding of statistical methods
Ability to critically analyze and interpret scientific data
Have an analytic and strategic mindset
Ability to work within tight deadlines, adjust to changes in priorities
Ability to function independently
Ability to identify problems and research possible solutions
Takes actions that are best for the company versus his or her individual unit
Encourages and supports information sharing and collaboration across teams and departments
Demonstrates sound business ethics; shows consistency among principles, values and
Strong ability to interpret and disseminate relevant clinical studies / medical product
Proficiency in MS Office applications and proficiency in or ability to learn EndNote or Reference Manager or other similar software tools needed for performing the
Basic understanding of regulatory compliance for medical

Your Background

English proficiency is required (C1).
Minimum of a Bachelor's degree or equivalent education in health, life sciences, engineering or a similar discipline MD, MS and PhD
Demonstrated authorship of scientific publications in peer review journals will be an
3-5 years of experience in medical writing, clinical affairs, regulatory affairs, or product engineering in the medical device industry required, with a strong preference to those with similar work experience in the orthopedic medical device
In lieu of the medical device industry experience, 3-5 years as a professor or senior investigator in a healthcare related field, with a demonstrated record of research and scientific

Travel Expectations

Up to 5%

EOE/M/F/Vet/Disability

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