Clinical Research Associate Job at Abbott, USA | Life Sciences Candidates, Apply Now

Clinical Research Associate Job at Abbott, USA | Life Sciences | Apply Now

If you are an experienced clinical operations professional or site manager looking to advance your career with a global healthcare leader, an opportunity within Abbott’s clinical affairs division is an exceptional milestone. Positions like the Clinical Research Associate I inject your regulatory and monitoring skillsets directly into advanced research settings—such as Abbott’s Diabetes Care hub in Alameda, California, or regional medical device pipelines. For detail-oriented specialists searching for a high-value Clinical Research Associate Job, these roles offer hands-on ownership of site monitoring phases, electronic Trial Master File (eTMF) architectures, and medical device accountability tracking. It serves as an elite launchpad for a long-term Abbott career and stands out as a premier choice for anyone tracking a competitive, compliance-driven CRA Job.

About The Company

Abbott is a global healthcare pioneer operating in over 160 countries, dedicated to creating life-changing technologies that span diagnostics, medical devices, nutritionals, and branded generic medicines. Recognized worldwide as a premier employer for scientists, Abbott pushes the boundaries of medical engineering—exemplified by milestone consumer sensor platforms like the FreeStyle Libre glucose monitoring network. Operating within Abbott’s Medical and Clinical Affairs division, CRAs support the complete lifecycle of clinical development. Working under rigorous regulatory frameworks, professionals ensure that clinical data from investigative sites is accurate, high-yielding, and fully optimized for health authority reviews and regulatory market submissions.

Clinical Research Associate Job – Key Responsibilities

As a Clinical Research Associate, your primary focus is to verify that patient safety, data integrity, and protocol compliance are strictly upheld across multiple assigned investigational centers.

Your core monitoring, regulatory documentation, and quality governance duties include:

• End-to-End Site Visits: Executing essential study site milestones, including Site Qualification (SQV), Site Initiation (SIV), Routine Interim Monitoring (IMV), and Close-Out Visits (COV), followed by the generation of formal monitoring reports.
• ICH-GCP and ISO Compliance: Auditing investigator site logs to guarantee absolute adherence to Study Protocols, Good Clinical Practices (GCPs), ISO 14155 (medical device standards), and applicable Code of Federal Regulations (CFR) guidelines.
• Device and Inventory Accountability: Managing the secure logistics, shipment, and physical device accountability of investigational supplies between localized warehouses and target clinical centers.
• TMF Governance & Inspection Readiness: Maintaing and auditing trial master file documentation within centralized eTMF platforms to maintain continuous, audit-ready status for this Clinical Research Associate Job.
• Data Listing Review & Query Resolution: Reviewing Case Report Forms (CRFs) and electronic clinical data listings for accuracy, resolving complex data discrepancies, and escalating anomalies to the Clinical Operations Manager or Study Lead.
• Start-Up Architecture: Collaborating with senior clinical staff to design trial-specific monitoring plans, customize Informed Consent Forms (ICFs), and facilitate investigator training workflows to advance this CRA Job.

Qualifications & Profile Requirements For Clinical Research Associate Job

Abbott’s clinical operations teams seek independent, detail-oriented communicators capable of fostering highly professional partnerships with principal investigators and site coordinators.

• Required Academic & Experience Criteria:
  • Educational Foundation: A formal Bachelor of Science (B.S.) degree in Life Sciences, Bioengineering, or a related quantitative scientific discipline.
  • Experience Tier: A minimum of 1 to 2+ years of direct experience operating as a Clinical Research Associate (CRA), Clinical Research Coordinator (CRC), or Clinical Trial Assistant (CTA) within the pharmaceutical or device industry.
  • Regulatory Grounding: Solid working comprehension of FDA regulations, CFR, and ICH-GCP guidelines to build a successful Abbott career.
  • Technical Agility: High proficiency across the Microsoft Office Suite and direct experience navigating clinical software, such as Clinical Trial Management Systems (CTMS) and electronic data capture portals.
• Preferred Assets:
  • Prior monitoring or coordination experience explicitly tied to medical device trials or in-vitro diagnostics (IVD) systems.
  • Active clinical research professional certifications (e.g., CCRA from ACRP or CCRP from SoCRA).

In short, securing a Clinical Research Associate position at Abbott is a definitive route to transitioning your scientific background into a high-visibility, industrial asset. Joining this elite tier allows you to step away from administrative data logging and actively steer the site relationships, device reconciliations, and regulatory eTMF workflows that advance life-saving medical breakthroughs into global consumer markets. If you possess a life sciences degree, meet the foundational trial experience thresholds, and maintain an uncompromising approach to quality standards, apply today to secure this premier Clinical Research Associate Job, launch a highly rewarding Abbott career, and lock in this outstanding CRA Job.

APPLY ONLINE HERE