Clinical Research Associate
United States of America : Remote
JOB DESCRIPTION:
About AbbottAbbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:
- Career development with an international company where you can grow the career you dream of.
- Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
- An excellent retirement savings plan with high employer contribution
- Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
- A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
- A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
This position works out remote in the Diagnostics Division.
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. We are seeking an experienced professional individual contributor to join our team. This role operates under limited supervision and requires the application of subject matter knowledge in Medical Affairs.
What You’ll Work On
As an experienced professional in the Medical Affairs Sub-Function, you will:
- Oversee the direction, planning, execution, and data collection activities of clinical trials/research.
- Contribute to the implementation of clinical protocols and facilitate the completion of final reports.
- Recruit clinical investigators and negotiate study design and costs.
- Direct human clinical trials (phases III & IV) for company products under development.
- Participate in adverse event reporting and safety monitoring.
- Coordinate and provide information for reports submitted to regulatory agencies.
- Monitor adherence to protocols and determine study completion.
- Coordinate and oversee investigator-initiated and group studies.
- Act as a consultant/liaison with other corporations under licensing agreements.
- Apply skills and knowledge to meet specific needs and requirements.
- Work independently while contributing to team goals.
EDUCATION AND EXPERIENCE YOU’LL BRING
Minimum Qualifications
- Associates Degree in sciences with a minimum 1 year of clinical research experience.
- ACRP Certification or CCRP Certification preferred
Learn more about our benefits that add real value to your life to help you live fully: http://www.abbottbenefits.com/pages/candidate.aspx. Follow your career aspirations to Abbott for diverse opportunities with a company that provides 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 Twitter @AbbottNews and @AbbottGlobal.
The base pay for this position is
$60,000.00 – $120,000.00In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Medical & Scientific Affairs
DIVISION:
CRLB Core Lab
LOCATION:
United States of America : Remote
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes, 25 % of the Time
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf Apply
Job Profile
Remote
Benefits/PerksCareer development Education benefit Education benefits Excellent retirement savings plan Freedom 2 Save student debt program Free medical coverage FreeU education benefit Great Place to Work Medical coverage Recognized as a great place to work Retirement savings plan Retirement savings plan with high employer contribution Student debt program Tuition reimbursement Work that matters
Tasks- Coordinate studies
- Data Collection
- Direct human clinical trials
- Implement clinical protocols
- Monitor adherence to protocols
- Oversee clinical trials
- Recruit clinical investigators
- Reporting
- Research
Adverse event reporting Branded generic medicines Clinical protocols Clinical Research Clinical trials Data Collection Diagnostics Education English Healthcare Investigator-initiated studies Medical Affairs Medical Devices Medical science Monitoring Negotiation Nutritionals Planning Regulatory Compliance Reimbursement Research Safety Monitoring Study Design
Experience1 years
EducationClinical research DO Healthcare Science
CertificationsACRP certification CCRP certification
TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9