Clinical Research Associate Job at Abbott, USA | Earn Upto $116,000.00 | Apply Online
If you are an experienced clinical trials professional looking to advance your career with a global healthcare leader, this full-time position at Abbott is an exceptional opportunity. Located entirely on-site at the medical device division in Alameda, California, this role embeds you directly within the rapidly expanding diabetes care and sensing technology business unit. For detail-oriented specialists searching for a high-value Clinical Research Associate Job, this position offers hands-on ownership of site monitoring visits, device reconciliation pipelines, and electronic Trial Master File (eTMF) architectures. It serves as an elite milestone for an Abbott Career and stands out as a premier choices for anyone tracking a high-growth, stable Life Sciences Job in the San Francisco Bay Area.
- Job Position: Clinical Research, Associate I
- Location: United States – California – Alameda
- Category:Â Research & Development
About The Company
Abbott is a global healthcare giant dedicated to helping people live more fully at all stages of life. Backed by a workforce of 115,000 colleagues serving patients across 160 countries, Abbott’s portfolio spans leading businesses in diagnostics, nutritionals, branded generic medicines, and medical devices.
About The Department
The Alameda campus houses Abbott’s pioneering Diabetes Care unit. This division is focused on revolutionizing the way people monitor their glucose levels with life-changing sensing technologies (such as the FreeStyle Libre platform), liberating over 500,000 individuals with diabetes from routine fingersticks. Working here means collaborating within an environment recognized worldwide as a top employer for diversity, scientists, and working mothers.
Clinical Research Associate Job – Key Responsibilities
As a Clinical Research Associate I, you will ensure the complete quality, accuracy, and clinical integrity of trial data throughout the full lifecycle of multiple medical device studies.
Your core monitoring, site management, and data compliance duties will include:
- Site Visit Execution: Performing critical internal and external study site visits—including Site Qualification (SQV), Site Initiation (SIV), Interim Monitoring (IMV), and Close-Out Visits (COV)—and generating formal monitoring reports.
- GCP & Regulatory Oversight: Conducting site management activities to guarantee absolute compliance with Study Protocols, Good Clinical Practices (GCPs), ICH guidelines, ISO14155, and Code of Federal Regulations (CFR) frameworks.
- Device Accountability: Managing the shipping of investigative study devices and supplies to clinical sites while performing precise device accountability and final inventory reconciliation.
- Study Start-Up Architecture: Participating in early-stage study start-up activities, including designing Case Report Forms (CRFs) and assisting senior staff with study-specific monitoring plans.
- TMF Governance & Inspection Readiness: Maintaining and auditing the Trial Master File (TMF) and uploading core documentation to the eTMF system to ensure continuous regulatory inspection readiness for this Clinical Research Associate Job.
- Data Listing Review: Reviewing clinical data listings for completeness and escalating discrepancies to the Clinical Operations Manager or Study Lead to secure a high-quality Life Sciences Job workflow.
Qualifications & Profile Requirements For Clinical Research Associate Job
This corporate position is tailored for analytical, highly organized communicators who possess the technical confidence to build exceptional rapport with clinical investigators and study site staff.
- Minimum Required Criteria:
- Educational Foundation: A Bachelor’s degree (BS) in a life sciences field or an equivalent combination of appropriate education and experience.
- Industry Track Record: A minimum of 2 years of direct experience operating as a Clinical Research Associate (CRA), Clinical Research Coordinator (CRC), or Clinical Trial Assistant (CTA).
- Technical Frameworks: A solid working knowledge of CFR, ICH-GCP guidelines, and basic clinical/regulatory affairs protocols.
- Computer Agility: High proficiency with Microsoft Office Suite (Word, Excel, Teams) and familiarity navigating electronic trial tracking tools.
- Preferred Assets:
- Prior experience conducting clinical trials specifically for medical devices or in-vitro diagnostics (IVD) systems to accelerate your Abbott Career.
- Background handling FDA inquiries, regulatory audits, or pre-submission data reviews.
Logistics, Base Salary & Corporate Benefits
Abbott structurally invests in the health, well-being, and financial security of its team members, providing a premier corporate benefits architecture:
- Location: Alameda, California, United States (100% On-Site / Office & Lab Link).
- Work Schedule: Regular Full-Time within Research & Development.
- Base Salary Scale: $73,900.00 – $116,000.00 annually (Final placement within this range depends on location-specific factors, prior device monitoring exposure, and technical credentials).
- Premium Health Incentives: Eligibility for free medical coverage within the Health Investment Plan (HIP) PPO medical plan in the subsequent calendar year.
- Financial & Retirement Security: An excellent retirement savings plan featuring high employer contribution matching.
- Education Incentives: Comprehensive tuition reimbursement programs, the Freedom 2 Save student debt relief initiative, and the FreeU program providing an affordable path to a bachelor’s degree.
In short, the Clinical Research Associate I position at Abbott is a definitive route to transitioning your foundational clinical tracking experience into a premium medical device asset. Securing this appointment allows you to step away from repetitive data logging and actively manage the site relationships, device reconciliations, and eTMF configurations that drive life-changing sensor innovations into global consumer markets. If you reside within a sustainable driving distance of Alameda, possess two years of verified CRA or coordinator experience, and want to build an elite corporate trajectory, apply today to secure this premier Clinical Research Associate Job, launch a highly rewarding Abbott Career, and lock in this outstanding Life Sciences Job.
