Senior Principal Scientist, Clinical Research

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.

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. 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 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 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 Sylmar, CA location in the Cardiac Rhythm Management division.

As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats.

Senior Principal Clinical Research Scientist , will be viewed as a leader on scientific and medical matters related to clinical trial design, clinical evaluations, risk management, strategy, management, and / or analysis of data. Expert in writing / managing clinical evaluation (plans and reports) or clinical trial protocols, risk master lists, clinical trial registrations and results postings, clinical study project timelines and scientific publications. Leads various study support groups and cross-functional teams in order to develop clinical strategy. Interacts with regulatory agencies as needed, and will use their scientific and medical knowledge in order to provide directives to teams as well as study sites. Be able to mentor other clinical scientists within Clinical Research.

What You'll Work On

Provide scientific leadership to the team, advising on different aspects of clinical evaluations and trial strategies, risk management, design, data analysis, and / or a variety of scenarios for a robust strategy and planning.

This position will require significant interactions with cross-functional teams within (Biostatics, RA, Clinical Operations, Data Management, Safety, Science, Clinical Affairs, etc) and outside (R&D, strategic marketing, Clinical R&D, Quality Engineering, Product Performance Group, Risk Management) clinical-regulatory organization, and some interactions with principal investigators in the trials.

Responsible for the delivery of the development of clinical evaluation plans or reports, and / or study protocols, the resulting reports and able to lead scientific discussions.

Interprets results in preparation for product applications by evaluating clinical and scientific and risk data and literature, and staying abreast of current clinical practice.

Presents scientific data by communicating accurate, succinct summaries of clinical results at industry gatherings, investigational meetings and regulatory agency meetings.

Facilitates regulatory submissions and communications by communicating with Regulatory Affairs during the submission process.

Participates in and supports audits.

Financial, budgetary, and legal interactions are expected as directed by the manager.

Responsible for compliance with applicable Corporate and Divisional Policies and procedures.

Will perform this job in a quality system environment.

Required Qualifications

Bachelors Degree in related field OR an equivalent combination of education and work experience

Minimum 10 years

At least 5 years of clinical trial, risk management, or clinical evaluation experience.

Comprehensive knowledge of specified functional area. Uses in-depth knowledge of business unit functions and cross group dependencies / relationships. Is recognized as an expert in work group and across functions. Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations. 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.

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 / Abbottand on Twitter @AbbottNews and @AbbottGlobal.

The base pay for this position is $146,700.00 $293,300.00. In specific locations, the pay range may vary from the range posted.