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Abbott

Makes heart devices, glucose sensors and lab tests

Clinical Research Associate 1

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeAlameda, CA, USA$73.9k - $116k

About the Job

Requirements

  • A Bachelor of Science degree in life sciences or equivalent, with at least one year of clinical research experience, or a combination of appropriate education and experience.
  • Experience working on medical device studies and/or in-vitro diagnostics studies is preferred; pharmaceutical background may also be considered.
  • Working knowledge of Code of Federal Regulations, International Council for Harmonisation Good Clinical Practice, and Clinical and Regulatory Affairs.
  • Proficiency with Microsoft Office suite.
  • Ability to travel 30–50%, with additional travel as required.

Responsibilities

  • Ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials according to the Code of Federal Regulations, International Council for Harmonisation Good Clinical Practice, and ISO 14155.
  • Perform study site visits, generate monitoring reports, and track resolution of action items.
  • Assist with and conduct clinical monitoring and site management activities, ensuring compliance with the study protocol, Good Clinical Practices, International Council for Harmonisation guidelines, Federal Regulations, department procedures, and other applicable regulatory requirements.
  • Participate in study start-up activities.
  • Assist with shipping study devices and supplies to clinical sites.
  • Perform study device accountability and reconciliation.
  • Assist senior staff in developing study-specific forms and trial-specific monitoring plans.
  • Assist senior staff in study planning, designing case report forms, and training study sites.
  • Maintain and audit the Trial Master File and upload materials to the electronic Trial Master File to ensure inspection readiness.
  • Review clinical data listings for completeness and accuracy and escalate issues to the Clinical Operations Manager or Study Lead as needed.
  • Communicate the status of clinical studies to management.
  • Participate in interim and final reviews of study data in preparation for regulatory submissions.
  • Interact with Regulatory Affairs and Quality Assurance in responding to audits and Food and Drug Administration inquiries as needed.
  • Perform other duties assigned by management.

Desired Qualifications

  • Demonstrated excellence in teamwork and solid interpersonal and communication skills, including building rapport with team members, peers, study site staff, and clinical management.
  • Flexibility in daily activities.

About the Company

Abbott

Makes heart devices, glucose sensors and lab tests

Abbott makes medical devices, diagnostic tests, nutrition products and branded generic drugs for hospitals, laboratories, pharmacies and patients. Its best-known product is the FreeStyle Libre, a coin-sized sensor worn on the upper arm that tracks blood sugar around the clock without routine finger pricks. Its other lines run from heart valves, pacemakers and brain stimulators to lab analyzers, rapid tests and mail-in colon cancer screening kits, and Abbott earns money by selling these products to health systems, labs, retailers and consumers. The company was founded in 1888 by Chicago physician Wallace Abbott and is based in Abbott Park, Illinois.

Company size
10,001+
Company stage
IPO
Headquarters
Abbott Park, IL
Founded
1888

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