Clinical Project Manager – Medical Devices
Location: Alameda, California, United States
Category: Medical and Clinical Affairs
About Abbott
Abbott is a global healthcare leader committed to helping people live healthier and fuller lives at every stage. Our portfolio spans diagnostics, medical devices, nutritionals, and branded generic medicines. With over 114,000 colleagues serving patients in more than 160 countries, Abbott is recognized for developing innovative, life-changing healthcare technologies that improve patient outcomes worldwide.
Abbott’s medical device division focuses on advancing clinical solutions in cardiovascular care, diabetes management, and chronic disease management through innovative and regulatory-compliant devices.
Position Overview
Abbott is seeking a Clinical Project Manager to join our Alameda, California team. This is an individual contributor role responsible for executing complex and specialized clinical projects, providing operational oversight, and mentoring junior clinical staff. The role requires experience in clinical trial management, regulatory compliance, and process optimization to ensure successful execution of clinical programs.
The Clinical Project Manager will work closely with cross-functional teams including R&D, Regulatory, Quality, and Clinical Operations to ensure studies are conducted efficiently, on time, and in accordance with Good Clinical Practice (GCP) and standard operating procedures (SOPs).
Key Responsibilities
Plan, direct, and communicate clinical study timelines and deliverables.
Collaborate with cross-functional teams to develop comprehensive project plans.
Ensure consistency of clinical study processes across multiple trials.
Oversee operational aspects of clinical trials, including investigational device release, site management, and protocol compliance.
Develop, refine, and implement SOPs; provide training to clinical staff and site personnel as required.
Monitor study progress and proactively resolve operational challenges.
Ensure clinical trials comply with regulatory requirements and Abbott policies.
Identify opportunities for process improvement and contribute to workflow optimization initiatives.
Support project leadership and provide mentorship to junior clinical staff.
Required Qualifications
Associate’s degree in Life Sciences, Healthcare, or a related field (Bachelor’s degree preferred).
Minimum 5–7 years of experience in clinical project management, preferably in the medical device or healthcare industry.
Strong knowledge of GCP, SOPs, and clinical trial regulations.
Demonstrated ability to manage complex projects and meet deadlines in a fast-paced environment.
Excellent written, verbal, and interpersonal communication skills.
Ability to travel up to 25–30% for site visits and project meetings.
Compensation
Base Pay: $86,700 – $173,300 (may vary by location and experience)
Why Join Abbott
Opportunities for professional growth in a global, innovative healthcare company.
Comprehensive benefits including healthcare, retirement, and wellness programs.
Chance to work on impactful clinical projects that improve patient outcomes worldwide.
Learn more about Abbott benefits at www.abbottbenefits.com.
Abbott is an Equal Opportunity Employer, committed to diversity and inclusion in the workplace.
This job posting is SEO and GEO optimized for global visibility on ThePharmaDaily.com, targeting clinical project management professionals seeking opportunities in medical devices and life sciences.
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