Senior Medical Writer

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.

Senior Medical Writer

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. Youll also have access to :

Career development with an international company where you can grow the career you dream of.

Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

An excellent retirement savings plan with a high employer contribution

Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelors degree.

A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.

A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

This position works out of our Plymouth MN OR St Paul, MN locations for our Electrophysiology division. In Abbotts Electrophysiology (EP) business, were advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives.

We have an exciting opportunity for the right candidate to join our rapidly growing clinical team within the EP division. The Medical Writer will be responsible for producing abstracts, manuscripts, scientific publications, and clinical study reports. This position will work collaboratively with clinical scientists, biostatisticians, marketing, and other cross-functional leads. This position will also play a supporting role in interacting with clinical trial investigators and clinicians to ensure the successful execution of clinical strategies to meet corporate podium and publication goals.

What You'll Work On

This position will work closely with cross-functional stakeholders in marketing, medical affairs, clinical affairs, biometrics, project management, data management, and other clinical groups. This position will also interact with physicians and regulatory authorities. Furthermore, this position will be required to execute the job responsibilities within the corporate policies and standard operating procedures. This position will :

Responsible and accountable for execution of presentations, scientific publications, clinical study report writing for regulatory submission in collaboration with clinical program director and scientists

Ensure cross-functional alignment of prioritization of clinical evidence dissemination

Effectively communicate information through the planning and execution of meetings and presentations and present recommendations to all stakeholders

Ensure internal stakeholders are up to date on all activities supporting podium presentations (conference acceptances, presentation status) and publications status as well as clinical study report review

Drive internal and external collaborators to meet submission deadlines for conferences and journal submissions

Drive activities to meet the deadlines for internal approvals of clinical study reports for regulatory submissions

Oversee responses to journal reviewers and ensure they are handled in a timely manner

Ensure all data presented is cohesive and in alignment with Abbott standards

Support publication committee activities (planning and strategy) for key trials

Plays a key role in KOL management through strategic engagement while maintaining a collaborative relationship

Develops and maintains current, in-depth, relevant functional knowledge (such as scientific and technical aspects) of projects in support of the business on a global basis

Will perform this job in a quality system environment.

Works with stakeholders to define business questions, requirements, timelines, objectives, and success criteria to address the need

Required Qualifications

Bachelor's degree required; advanced degree preferred; degree in science, medicine, or a similar discipline is highly preferred.

Minimum of 5+ years of related work experience in clinical trials / medical writing

Cardiovascular knowledge is a plus.

What We Offer

At Abbott, you can have a good job that can grow into a great career. We offer :

A fast-paced work environment where your safety is our priority

Training and career development , with onboarding programs for new employees and tuition assistance

Financial security through competitive compensation, incentives and retirement plans

Health care and well-being programs including medical, dental, vision, wellness and occupational health programs

Paid time off

401(k) retirement savings with a generous company match

The stability of a company with a record of strong financial performance and history of being actively involved in local communities

Apply Now

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives : www.abbottbenefits.com

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com, on Facebook at www.facebook.com / Abbott, and on X @AbbottNews.

The base pay for this position is $97,300.00 $194,700.00. In specific locations, the pay range may vary from the range posted.