Clinical Project Lead

JOB DESCRIPTION:

About Us:At Abbott we help people live more fully at all stages of life. Abbott is about the power of health. For more than 130 years Abbott has been helping people reach their potential because better health allows people and communities to achieve more. With a diverse global network serving customers in more than 160 countries we create new solutions across the spectrum of health around the world for all stages of life. Whether its next-generation diagnostics life-changing devices science-based nutrition or novel reformulations we are advancing some of the most innovative and revolutionary technologies in healthcare helping people live their best lives through better health.

Abbott Diabetes Care designs develops and manufactures leading-edge glucose monitoring technology for use in both home and hospital settings including our revolutionary Freestyle Libre Flash Glucose Monitoring System.

About the Role:

As aClinical Project Leadwithin Abbott Diabetes Cares Clinical Affairs team you will play a pivotal role in driving the success of our clinical programs.

Responsibilities:

As aClinical Project Leadwithin Abbott Diabetes Cares Clinical Affairs function you will:

• Lead cross-functional project teams in the planning execution and close-out of clinical trials.

• Ensure clinical support is aligned with the needs of R&D Marketing Operations Quality Assurance and Regulatory Affairs.

• Develop and implement strategic plans for clinical study delivery using both internal and external resources.

• Manage relationships with clinicians CROs Key Opinion Leaders (KOLs) and other stakeholders to ensure successful project outcomes.

• Serve as the primary point of contact for internal updates issue resolution financial reconciliation and project timeline tracking.

• Collaborate with internal teams including Data Management Regulatory Statistics and Scientific Affairs to ensure seamless project execution.

• Contribute to the evaluation of new or modified Abbott Diabetes Care and competitor products through clinical studies.

• Maintain focus on key milestones stakeholder engagement and compliance with regulatory and quality standards.

Education and Experience

• A degree in Life Sciences or a related field is preferred; however candidates with strong relevant experience and alternative educational backgrounds will also be considered.

• Experience in the medical device or in vitro diagnostics (IVD) industry is highly desirable; pharmaceutical experience may also be considered.

• Proven background in clinical project management or study leadership ideally within a regulated environment.

• Strong communication time management and problem-solving skills.

• Ability to thrive in a fast-paced collaborative environment.

• Willingness to travel up to 10% with the remainder of the time based at our Manufacturing Centre of Excellence and R&D facility in Witney Oxfordshire.

What We Offer

At Abbott we believe in helping you bring your passion ideas and purpose to return we offer:

• A competitive salary and benefits package.

• A class-leading defined contribution pension scheme.

• Share ownership opportunities.

• A supportive and inclusive work environment that encourages career growth and development.

• Access to a wide range of wellness initiatives and employee engagement activities:

  • At our Witney site: onsite allotments couch-to-5k campaigns beekeeping yoga and more.

Join us and shape your career as you help shape the future of healthcare.

Connect with us at or on LinkedIn at on Facebook at and on Twitter @AbbottNews.

Abbott is an equal opportunities employer.

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The base pay for this position is

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

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