Job Title:
Senior Medical Writer
Company:
Abbott Laboratories
Category:
Medical and Clinical Affairs
Locations:
Plymouth, MN
St. Paul, MN
(Electrophysiology Division)
About Abbott:
Abbott is a global healthcare leader helping people live more fully at all stages of life through life-changing technologies in:
Diagnostics
Medical Devices
Nutritionals
Branded Generic Medicines
With over 114,000 employees in 160+ countries, Abbott has been recognized as:
One of the World’s Most Admired Companies (Fortune)
A Great Place to Work globally
A Top Employer for diversity, women, and scientists
About the Division (Electrophysiology):
Abbott’s Electrophysiology (EP) business advances the treatment of heart disease and atrial fibrillation through breakthrough medical technologies that restore health and improve lives.
Position Overview:
The Senior Medical Writer will be responsible for creating and managing high-quality scientific documents and clinical communications, including:
Abstracts
Manuscripts
Scientific publications
Clinical study reports (for regulatory submission)
This role involves cross-functional collaboration with clinical scientists, biostatisticians, marketing, and regulatory teams, as well as interactions with clinicians and investigators to support clinical publication strategies.
Key Responsibilities:
Scientific & Clinical Writing
Prepare presentations, manuscripts, publications, and clinical study reports in collaboration with clinical program directors and scientists.
Ensure accuracy, clarity, and compliance with Abbott’s scientific and regulatory standards.
Manage responses to journal reviewers and ensure timely resolution.
Project & Publication Management
Oversee conference submissions, journal publications, and regulatory report approvals.
Coordinate cross-functional reviews to maintain consistency and alignment.
Track and communicate project status (e.g., conference acceptances, publication progress).
Support publication committee activities including strategy and planning.
Collaboration & Communication
Work closely with internal teams (marketing, clinical, biometrics, project/data management).
Engage with physicians, investigators, and regulatory authorities.
Facilitate effective meetings and presentations across stakeholders.
Strategic & Technical Support
Maintain up-to-date scientific and technical knowledge relevant to Abbott’s EP projects.
Support KOL (Key Opinion Leader) management through strategic engagement.
Ensure all presented data aligns with corporate quality and ethical standards.
Required Qualifications:
Bachelor’s degree required; advanced degree (Master’s/Ph.D.) preferred.
Field: Science, Medicine, or related discipline (highly preferred).
Minimum 5+ years of experience in clinical trials or medical writing.
Cardiovascular knowledge is a plus.
Key Skills:
Strong scientific writing and editing skills
Excellent communication and organizational abilities
Familiarity with regulatory and publication processes
Ability to manage multiple priorities and deadlines
Work Environment:
Operates within a Quality System Environment following company SOPs and regulatory standards.
Compensation:
Base Pay Range: $97,300 – $194,700 (may vary by location)
Employee Benefits:
Free Medical Coverage (HIP PPO Plan)
Retirement Savings Plan with high employer contribution
Tuition Reimbursement and Freedom 2 Save program
FreeU Education Benefit for affordable bachelor’s degree completion
Comprehensive Health & Wellness Programs (medical, dental, vision, occupational health)
Paid Time Off and 401(k) with generous company match
Career development and international growth opportunities
Equal Opportunity Statement:
Abbott is an Equal Opportunity Employer committed to diversity, inclusion, and fair employment practices.
Application Links:
🌐 Website: www.abbott.com
👥 Facebook: facebook.com/Abbott
🐦 X (Twitter): @AbbottNews
💼 Benefits: www.abbottbenefits.com
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