Abbott Clinical Research Associate in Lake Forest, Illinois
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines. Our 109,000 colleagues serve people in more than 160 countries.
About Abbott Diagnostics
Diagnostic testing is a compass, providing information that helps in the prevention, diagnosis and treatment of a range of health conditions.
Abbott’s life-changing tests and diagnostic tools give you accurate, timely information to better manage your health. We’re empowering smarter medical and economic decision making to help transform the way people manage their health at all stages of life. Every day, more than 10 million tests are run on Abbott’s diagnostics instruments, providing lab results for millions of people.
Our location in Lake Forest, Illinois currently has an opportunity for a Clinical Research Associate .
This is an in-house role, incumbent must be onsite.
WHAT YOU’LL DO
The Clinical Research Associate (CRA) designs, implements and monitors clinical studies of new and modified in vitro diagnostics products. Ensures that the clinical studies are designed to validate product performance claims and supports products ‘intended use. Prepares clinical data reviews and data summaries. Participates in the preparation of regulatory submissions and international registration packages. In general, the CRA performs responsibilities and tasks under the direction of a SCRA or CPM.
Main responsibilities include:
Implements and maintains the effectiveness of the Quality System.
Complies with all policies, established procedures and regulations related to clinical research
Actively participates as a member of the cross-functional project team
Assesses data generated by R&D/Business Teams
Prepares design validation plans
Prepares documents for clinical studies
Identifies and qualifies clinical investigators and clinical sites
Proposes and negotiates budgets for clinical studies; initiates payments to sites
Obtains and reviews all required essential documents necessary for study initiation
Reviews data, prepares and presents clinical data reviews and data summaries
Responds to audits and data queries
Prepares the clinical sections of regulatory submissions and international registration packages
Assists Regulatory in preparing responses to regulatory agencies’ questions regarding the clinical study
Acquires a basic understanding of the principles of the assay and/or instrument and “hands-on” knowledge and skills in performing assigned assays or operating instruments
Arranges for and assists in standard Statistical Support with the collection and statistical analyses of clinical data
Monitors standard clinical studies ensuring site compliance with the clinical protocol and ICH/GCP guidelines, assures subject rights, safety, and welfare is protected, ensures data integrity through completeness, accuracy and legibility
Prepares and reviews product labeling and promotional materials
Conducts standard pre-study initiation, interim and close-out monitoring site visits and completes site visit reports
Initiates standard clinical studies and provides for investigator and staff training
Maintains accurate and timely sponsor/site correspondence and communication
Prepares and presents project progress reports to keep management and team informed
Supports publication or presentation of clinical data in professional journals or meetings
Maintains professional, product and market expertise via independent reading, networking and training
Implements all policies, established procedures and regulations into daily operations as appropriate
Develops professional expertise via professional and educational opportunities
Assumes responsibility for attending training sessions, presentations and continuing education sessions
Works with assistance to prepare publications, abstracts or presentations for professional meetings
Accepts and completes all management-directed work assignments such as clinical assignments, travel and other tasks
EDUCATION AND EXPERIENCE YOU’LL BRING
Bachelor’s degree B.S in biological sciences or medical specialty preferred.
Minimum 3 years of clinical related experience
Knowledge of regulations and standards (GCP) affecting IVDs and Biologics
Clinical Laboratory certification (MT, ATCP or equivalent) or certification as a clinical research associate (CCRA)
Site monitoring of investigational drug or device trials or clinical laboratory assay/instrument experience
Demonstrates good basic writing and presentation skills (i.e. clear, concise, effective and well organized)
WHAT WE OFFER
At Abbott, you can have a good job that can grow into a great career. We offer:
A fast-paced work environment where your safety is our priority (Include for Manufacturing roles only)
Production areas that are clean, well-lit and temperature-controlled (Include for Manufacturing roles only)
Training and career development , with onboarding programs for new employees and tuition assistance
Financial security through competitive compensation, incentives and retirement plans
Health care and well-being programs including medical, dental, vision, wellness and occupational health programs
Paid time off
401(k) retirement savings with a generous company match
The stability of a company with a record of strong financial performance and history of being actively involved in local communities
Learn more about our benefits that add real value to your life to help you live fully: www.abbottbenefits.com (http://www.abbottbenefits.com/pages/candidate.aspx)
Follow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com , on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call 224-667-4913 or email firstname.lastname@example.org
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