Abbott Laboratories
Senior Director, Clinical Study Management
Abbott Laboratories, Santa Clara, California, us, 95053
Senior Director, Clinical Study Management page is loaded## Senior Director, Clinical Study Managementlocations:
United States - California - Santa Claratime type:
Full timeposted on:
Posted Todaytime left to apply:
End Date: February 9, 2026 (27 days left to apply)job requisition id:
31126082Abbott 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.## **JOB DESCRIPTION:****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* 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
student debt program and
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**Management overseeing a global portfolio of 100+ clinical studies across six business units in our Medical Devices division.a mission-driven portfolio that impacts patient lives globally. Work in a collaborative, innovative, and growth-oriented environment. Gain executive visibility and influence across multiple business units.**What You’ll Work On*** Lead the project management of global clinical trials with budgets exceeding $100MM.* Influence study design allowing for seamless study execution.* Drive strategic execution of clinical and regulatory goals across diverse therapeutic areas.* Manage timelines, budgets, and resources across a complex, multi-BU portfolio.* Collaborate with global teams to ensure regulatory compliance and operational excellence.* Mentor and develop a high-performing team of project managers and clinical professionals.* Operational Excellence Through Milestone Management: Oversee 400+ annual study milestones with a continuous improvement mindset—leveraging data and feedback loops to enhance efficiency, predictability, and execution quality.* Upstream Clinical Protocol Influence: Engage early in protocol development to ensure operational feasibility, minimize downstream challenges, and optimize business outcomes.* Strategic Business Partnership: Serve as a strategic partner to the business by aligning clinical operations with long-term regulatory and reimbursement goals. Influence study design to support future approvals and market access.* Strong Understanding of the Global Regulatory Landscape: Bring deep knowledge of international regulatory requirements to guide operational decisions.**Qualifications*** Bachelor’s degree in life sciences required* Advanced degree preferred* 7+ years of experience required leading large-scale, pre-market clinical trials in the medical device industry* Proven success required managing global studies and large budgets* Experience in vascular or cardiovascular devices is a plus* Strong leadership, communication, and cross-functional collaboration skillsLearn more about our health and wellness benefits, which provide the security to help you and your family live full lives: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 , on Facebook at
and on Twitter @AbbottNews and @AbbottGlobal**The base pay for this position is**$218,700.00 – $437,300.00In specific locations, the pay range may vary from the range posted.## **JOB FAMILY:**Research and Discovery## **DIVISION:**MD Medical Devices## **LOCATION:**United States > Santa Clara : Building A - SC## **ADDITIONAL LOCATIONS:**## **WORK SHIFT:**Standard## **TRAVEL:**Yes, 20 % of the Time## **MEDICAL SURVEILLANCE:**Not Applicable## **SIGNIFICANT WORK ACTIVITIES:**Keyboard use (greater or equal to 50% of the workday)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.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO\_Spanish.pdf #J-18808-Ljbffr
United States - California - Santa Claratime type:
Full timeposted on:
Posted Todaytime left to apply:
End Date: February 9, 2026 (27 days left to apply)job requisition id:
31126082Abbott 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.## **JOB DESCRIPTION:****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* 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
student debt program and
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**Management overseeing a global portfolio of 100+ clinical studies across six business units in our Medical Devices division.a mission-driven portfolio that impacts patient lives globally. Work in a collaborative, innovative, and growth-oriented environment. Gain executive visibility and influence across multiple business units.**What You’ll Work On*** Lead the project management of global clinical trials with budgets exceeding $100MM.* Influence study design allowing for seamless study execution.* Drive strategic execution of clinical and regulatory goals across diverse therapeutic areas.* Manage timelines, budgets, and resources across a complex, multi-BU portfolio.* Collaborate with global teams to ensure regulatory compliance and operational excellence.* Mentor and develop a high-performing team of project managers and clinical professionals.* Operational Excellence Through Milestone Management: Oversee 400+ annual study milestones with a continuous improvement mindset—leveraging data and feedback loops to enhance efficiency, predictability, and execution quality.* Upstream Clinical Protocol Influence: Engage early in protocol development to ensure operational feasibility, minimize downstream challenges, and optimize business outcomes.* Strategic Business Partnership: Serve as a strategic partner to the business by aligning clinical operations with long-term regulatory and reimbursement goals. Influence study design to support future approvals and market access.* Strong Understanding of the Global Regulatory Landscape: Bring deep knowledge of international regulatory requirements to guide operational decisions.**Qualifications*** Bachelor’s degree in life sciences required* Advanced degree preferred* 7+ years of experience required leading large-scale, pre-market clinical trials in the medical device industry* Proven success required managing global studies and large budgets* Experience in vascular or cardiovascular devices is a plus* Strong leadership, communication, and cross-functional collaboration skillsLearn more about our health and wellness benefits, which provide the security to help you and your family live full lives: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 , on Facebook at
and on Twitter @AbbottNews and @AbbottGlobal**The base pay for this position is**$218,700.00 – $437,300.00In specific locations, the pay range may vary from the range posted.## **JOB FAMILY:**Research and Discovery## **DIVISION:**MD Medical Devices## **LOCATION:**United States > Santa Clara : Building A - SC## **ADDITIONAL LOCATIONS:**## **WORK SHIFT:**Standard## **TRAVEL:**Yes, 20 % of the Time## **MEDICAL SURVEILLANCE:**Not Applicable## **SIGNIFICANT WORK ACTIVITIES:**Keyboard use (greater or equal to 50% of the workday)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.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO\_Spanish.pdf #J-18808-Ljbffr