Senior Staff Medical Writer

Job not on LinkedIn

🔥 0 minutes ago

🌵 Arizona, California, +3 more states – Remote

🌵 Arizona – Remote 🏄 California – Remote ⛰️ Colorado – Remote 🌲 Oregon – Remote ☕ Washington – Remote

💵 $110.1k - $238.4k / year

⏰ Full Time

🟠 Senior

🏥📝 Medical Writer

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Stryker

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1941

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Stryker is a global leader in medical technology, providing innovative products and services across the healthcare sector. With a presence in countries across the Americas, Asia Pacific, Europe, and the Middle East & Africa, Stryker offers a wide range of medical technologies, including orthopedic implants, surgical equipment, and advanced hospital devices. The company is committed to improving patient outcomes and healthcare efficiency. Stryker continues to expand its global reach, offering localized solutions to meet diverse healthcare needs worldwide.

📋 Description

• Author and maintain Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-Up (PMCF) documents, and other clinical evidence documentation supporting international product registrations and lifecycle management • Compile, analyze, and synthesize clinical evidence from clinical studies, published literature, post-market data, and other safety and performance sources into submission-ready regulatory documents • Respond to notified body reviews and regulatory feedback, driving resolution of clinical documentation questions to support ongoing market access • Collaborate with Regulatory Affairs, Clinical Affairs, Quality, Research & Development, and Marketing teams to develop clinical evidence strategies, regulatory documentation plans, and project timelines • Author clinical study protocols, study reports, data summaries, and supporting scientific documents • Conduct systematic literature reviews, evaluate scientific data, and integrate findings into clinical and regulatory documentation • Lead document review cycles, coordinate stakeholder feedback, resolve content issues, and obtain timely approvals • Drive continuous improvement initiatives, maintain medical writing tools and templates, and mentor junior medical writing team members

🎯 Requirements

• Required Bachelor’s degree in a scientific, technical, healthcare, or related discipline • Minimum 6 years of industry experience within medical technology, medical devices, pharmaceuticals, or healthcare products • Minimum 4 years of experience in scientific writing, medical writing, clinical research, or related regulatory documentation activities • Experience authoring Clinical Evaluation Reports (CERs) and Post-Market Clinical Follow-Up (PMCF) documentation • Expert knowledge of MEDDEV 2.7/1 Rev. 4, European Union Medical Device Regulation (EU MDR 2017/745), and MDCG guidance for clinical evaluations • Experience conducting systematic literature reviews and utilizing scientific databases, literature search methodologies, and literature management tools • Knowledge of FDA, Good Clinical Practice (GCP), ISO 14155, ISO 14971, and applicable international medical device regulations and standards • Preferred Master’s degree, PhD, PharmD, MD, MPH, RN, BSN, or other advanced health-related degree • Experience authoring clinical study protocols, clinical study reports, manuscripts, or scientific publications • Experience supporting regulatory submissions and global market access initiatives for medical devices • Knowledge of clinical operations, risk management, and international regulatory requirements

🏖️ Benefits

• Remote work arrangement • Equal opportunity employment • 10% travel