San Diego, California, USA
3 days ago
Director, U.S. Clinical Affairs

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. You’ll also have access to:

Career development with an international company where you can grow the career you dream ofEmployees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar yearAn excellent retirement savings plan with high employer contributionTuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degreeA 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 FortuneA 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

Our rapid diagnostics solutions are helping address some of the world’s greatest healthcare challenges. This Director will be a highly experienced manager, whose decisions tend to be more tactical and operational, is accountable for budget and policy recommendations and medium-term planning.

What You’ll Work On

Designs and provides oversight of clinical research programs.Builds relationships with key opinion leaders and applies their input to enhance study design and protocols.Assures that clinical research program design meets scientific objectives and is aligned with commercial needs.Ensure all clinical trials comply with Good Clinical Practice (GCP) guidelines and relevant regulatory standards.Manage clinical trial budgets, timelines, and resources effectively to ensure successful trial completion.Establishes the conditions essential for determining the safety, efficacy, medical usefulness, and marketability of drug or medical device products candidates.Interprets results of Phase I-IV investigations in preparation for new-drug or medical device application.May serve as safety expert for individual clinical projects.

Required Qualifications

Bachelor's degree in a relevant fieldMinimum 7 years of experience in a relevant fieldIn-vitro diagnostics (IVD) industry experience

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 $169,300.00 – $338,700.00. In specific locations, the pay range may vary from the range posted.

Confirm your E-mail: Send Email