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Abbott

Manager, Clinical Education

Posted 2 days ago
$99300 - $198K per year
5-10 years experience
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AI Summary

The manager oversees strategy implementation, operations, and clinical trial execution for the Medical Affairs sub-function. They are responsible for directing human clinical trials, managing data collection, and ensuring adherence to regulatory protocols.

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 122,000 colleagues serve people in more than 160 countries.

     

JOB DESCRIPTION:

Job Title

Manager, Clinical Education


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 of which you dream.
  • 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 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 

 

We are seeking a Clinical Education Manager for our Vascular division. This is a fully REMOTE role.  


Abbott Vascular provides innovative, minimally invasive and cost-effective products for treatment of vascular disease. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents

 

What You’ll Work On

 

Manages teams within the Medical Affairs Sub-Function.

Focus is on policy and strategy implementation and control rather than development.

Typically handles short-term operational/tactical responsibilities.

 

Core Job Responsibilities

 

  • As the Manager of the Medical Affairs Sub-Function, oversees the strategy implementation and operations for overseeing the direction, planning, execution, clinical trials/research and the data collection activities.
  • Contributes to implementation of clinical protocols, and facilitates completion of final reports.
  • Recruits clinical investigators and negotiates study design and costs.
  • Responsible for directing human clinical trials, phases III & IV for company products under development.
  • Participates in adverse event reporting and safety responsibilities monitoring.
  • Coordinates and provides reporting information for reports submitted to the regulatory agencies.
  • Monitors adherence to protocols and determines study completion.
  • Coordinates and oversees investigator initiations and group studies.
  • May participate in adverse event reporting and safety responsibilities monitoring.
  • May act as consultant/liaison with other corporations when working under licensing agreements

 

Education and Experience you’ll bring

  • Bachelor's degree, discipline appropriate to the project environment, clinical research, scientific and technical degree is preferred.
  • 5 years of related work experience with a good understanding of specified functional area, or Master's degree with 3 years of related work experience.
  • Experience as a CRA, direct clinical research experience, or an equivalent combination of education and work experience.  Medical Device/Diagnostics clinical experience is strongly preferred. Management experience in other clinical operations positions desirable.
  • Knowledge of regulations and standards affecting IVDs (In Vitro Diagnostics) and Biologics.
  • Has successfully led several high complexity projects.
  • Certifications from the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA) preferred.

 

  

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 Twitter @AbbottNews and @AbbottGlobal.

     

The base pay for this position is

$99,300.00 – $198,700.00

In specific locations, the pay range may vary from the range posted.

     

JOB FAMILY:

Medical & Scientific Affairs

     

DIVISION:

AVD Vascular

        

LOCATION:

United States of America : Remote

     

ADDITIONAL LOCATIONS:

     

WORK SHIFT:

Standard

     

TRAVEL:

Yes, 15 % of the Time

     

MEDICAL SURVEILLANCE:

No

     

SIGNIFICANT WORK ACTIVITIES:

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)

     

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

     

EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf

     

EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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