Senior Principal Clinical Scientist

in Plymouth, MN

Senior Principal Clinical Scientist Job

Job Description Job Attributes+

  • Job ID

    31081355

  • Req #

    ABLAUS31081355ENUSEXTERNAL

  • Job Location

    Plymouth, MN, US

  • Job Category

    Medical and Clinical Affairs

  • Job Type

    Full time

  • Travel

    Yes, 5 % of the Time

  • Schedule

    40 hours per week

Senior Principal Clinical Scientist

Working at Abbott

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

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

·       Free medical coverage for employees* via the Health Investment Plan (HIP) PPO

·       An excellent retirement savings plan with high employer contribution

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

·       A company recognized as a great place to work in dozens of countries around the world 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 a best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

This position works out of our Plymouth, MN location, supporting our Electrophysiology medical device division. The Senior Principal Clinical Scientist will lead scientific activities associated with the design, conduct, and reporting of clinical trials for this therapeutic area. In Abbott’s Electrophysiology (EP) business, we’re 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.

What You’ll Work On:

This position will work closely with the clinical study team including project management, biostatistician, data management, and other clinical study personnel. This position will have significant interaction with leadership and regulatory authorities. Furthermore, this position will be required to execute their job responsibilities within the corporate policies and standard operating procedures.  Additionally:

·       Develops, writes, or mentors others in creation of clinical strategy, risk management, or clinical evaluation planning for products and process changes, to gain regulatory approval for product release, additional claims or indications, by addressing issues from a clinical, medical, and scientific perspective and by interacting with appropriate personnel.

·       Develops, writes, or mentors others in generation of study-related documents and/or contribute content and oversight of such documents, including, but not limited to, clinical study reports, clinical study protocols, case report forms, investigational brochures, and informed consent forms.

·       Designs or mentors others in the design of clinical trials and studies in collaboration with internal stake holders including clinical project management, clinical operations, biostatistics data management, regulatory affairs, medical affairs as well as external stake holders including steering and publication committees.

·       Develop the scientific podium and publication strategy in close collaboration with cross-functional teams and lead the execution of the publication strategy through coordination with investigator authors and internal teams.

·       Serve as an active member of study teams and provide scientific support to justify trial design and ongoing scientific analysis during protocol development. May include generation of pre-protocol documentation of scientific information.

·       Review and critically analyze statistical analysis plans.

·       Generate documents to support regulatory submissions for Abbott products and/or respond to questions from regulatory authorities about existing submissions.

Required Qualifications: 

·       Advanced degree in the sciences, medicine, or similar discipline.

·       8+ years of related work experience with a solid understanding of specified functional area, or an equivalent combination of education and work experience.  

·       Demonstrated scientific writing ability.

·       Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations.

·       Independent decision making required.

·       Works on complex problems where analysis of situations or data requires an in-depth evaluation of various factors.

·       Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results.

·       Has broad knowledge of various technical alternatives and their potential impact on the business.

Preferred Qualifications:

·       PhD degree in the sciences, medicine, or similar discipline preferred.

·       Experience working on regulated, pre-market clinical studies preferred.

·       Experience working in a quality system environment preferred.

* Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.

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, on LinkedIn at https://www.linkedin.com/showcase/abbott-cardiovascular/ and on X (Twitter) @AbbottNews and @AbbottGlobal.



The base pay for this position is $109,300.00 – $218,700.00. In specific locations, the pay range may vary from the range posted.

Job Skills

  • clinical strategy
  • protocol development
  • project management
  • clinical trials
  • scientific writing
  • medical devices
  • medical affairs
  • regulatory affairs
  • biostatistics data management
  • biostatistics

 

Sorry, this job is closed.

Additional Information

Who We Are

PUT YOUR TALENTS TO WORK

Abbott values the leadership skills developed through military service and we have a broad range of functional areas to put your talents to work. Our organization is making a difference in the lives of the people we serve with a diverse offering of healthcare products. We have a strong veteran employee community to help with your transition from the military to the corporate world.

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