Join to apply for the Clinical Research Associate (Illinois) role at Abbott About Abbott 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 114,000 colleagues serve people in more than 160 countries. Abbott is a global healthcare leader creating breakthrough science to improve people’s health, always looking towards the future and anticipating changes in medical science and technology. Our diagnostic solutions are used in hospitals, laboratories, and clinics around the globe, providing crucial information that drives patient care decisions for a wide range of conditions. Working at Abbott 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 earning a bachelor’s degree. A company recognized as a top workplace in dozens of countries, named one of the most admired companies by Fortune, and celebrated for diversity, inclusive leadership, and support for working mothers and female executives. The Opportunity This is a remote position. Qualified candidates must currently live in the Chicagoland area. Must be able to travel up to 35%. What You’ll Work On Experienced professional individual contributor working under limited supervision. Applies subject‑matter knowledge in Medical Affairs, oversees clinical trial and research planning, execution, and data collection, and ensures regulatory compliance and safety monitoring. Oversight of the direction, planning, execution, clinical trials/research, and data collection activities. Contributes to the implementation of clinical protocols and facilitates completion of final reports. Recruits clinical investigators and negotiates study design and costs. Directs human clinical trials, phases III & IV, for company products under development. Participates in adverse event reporting and safety responsibilities monitoring. Coordinates and provides reporting information for regulatory submissions. Monitors adherence to protocols and determines study completion. Coordinates investigator initiations and overviews group studies. May act as consultant/liaison with other corporations under licensing agreements. Required Qualifications Associate’s degree Minimum 1 year of clinical research experience Preferred Qualifications Health science or life sciences experience CCRP (Certified Clinical Research Professional) or clinical association certification as a plus Abbott is an Equal Opportunity Employer, committed to employee diversity. Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: The base pay for this position is $60,000.00 – $120,000.00. In specific locations, the pay range may vary from the posted range. #J-18808-Ljbffr Abbott
...collaborative environment? As an experienced Epic Interface PM you will have the ability to share new ideas and collaborate on projects as a consultant without the extensive... ...Making Responsibilities+ Analytical ability to manage multiple projects and prioritize tasks into...
...aptitude with the ability to learn quickly and support software applications. Understanding of the technical components of an Information System, including basic hardware, platform, database concepts, and terminology. Ability to manage multiple priorities in a dynamic...
Job Title: School Office/Attendance Clerk, Elementary, Middle, and High SchoolJob Code: 145Grade: CDOT Code: 203362010Prepared By: Nathaniel AdamsPrepared Date: July 18, 2021Approved By: Leisa G. WoolfolkApproved Date: July 27, 2021SUMMARYCollect and...
...PD-1 with the anti-angiogenesis effects associated with blocking VEGF into a single molecule... ...PD-1 and VEGF. Summit has begun its clinical development of ivonescimab in non-small... .... Overview of Role The Clinical Research Associate (CRA) is responsible for supporting...
...Temporary Care Coordinator Sentara Health Plans is hiring a Temporary Care Coordinator for the Northern/Central Virginia area! Position... ...Requires Both In Person Face-to-Face Assessments and Remote Telephonic Assessments! Applicants Must Be Located in Western...