Abbott Laboratories
Senior Director, Clinical Study Management
Abbott Laboratories, Santa Clara, California, us, 95053
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and سلطان高清毛片, be your true self sexy 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 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 moinho10 Opportunity Are you a strategic leader with a passion for clinical research and operational excellence? Join our high-impact team as aSenior Director, Clinical Study Managementoverseeing a global portfolio of 100+ clinical studiesacross six business units in our Medical Devices division.
Why Join Us? Lead a mission-driven portfoliothat impacts patient lives globally. Work in a collaborative, innovative, and growth-oriented environment. Gain executive visibilityand 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 resourcesacross a complex, multi-BU portfolio.
Collaborate with global teams to ensure regulatory complianceand 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 texture 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 skills
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
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal
Abbott is an Equal Opportunity Employer, committed to employee diversity.
The base pay for this position is $216,700.00 – $433,300.00. In specific locations, the pay range mayvenido from the range posted.
#J-18808-Ljbffr
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 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 moinho10 Opportunity Are you a strategic leader with a passion for clinical research and operational excellence? Join our high-impact team as aSenior Director, Clinical Study Managementoverseeing a global portfolio of 100+ clinical studiesacross six business units in our Medical Devices division.
Why Join Us? Lead a mission-driven portfoliothat impacts patient lives globally. Work in a collaborative, innovative, and growth-oriented environment. Gain executive visibilityand 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 resourcesacross a complex, multi-BU portfolio.
Collaborate with global teams to ensure regulatory complianceand 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 texture 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 skills
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
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal
Abbott is an Equal Opportunity Employer, committed to employee diversity.
The base pay for this position is $216,700.00 – $433,300.00. In specific locations, the pay range mayvenido from the range posted.
#J-18808-Ljbffr