Clinical Research Coord III

Description:
Could you be our next Clinical Research Coordinator III with LIMR/Main Line Health?

Why work as a Clinical Research Coordinator III with Main Line Health?

• Make an Impact! Do you want a career where you can help others and make an impact? The Clinical Research Coordinator III independently manages and oversee the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP). Responsibilities included overseeing the execution of a study procedures as outlined by the study protocol (and related documents), screening for and managing the review of medical records and other sources for eligible research patients.
• Develop and Grow your Career! Invest in furthering your education through seeking certifications or advanced degrees by taking advantage of our Tuition Reimbursement! This position is eligible for up to $6,000 per year based upon your Full or Part Time status.
• Join the Team! Like our patients, the Main Line Health Family encompasses a wide range of backgrounds and abilities. Just as each of our patients requires a personalized care plan, each of our employees, physicians, and volunteers, bring distinctive talents to Main Line Health. Regardless of our unique design, we all share a purpose: providing superior service and care.
• Position-Specific Benefits include: You are eligible for up to 160 hours of paid time off per year based on your Full or Part Time status. We also offer a number of employee discounts to various activities, services, and vendors... And employee parking is always free!

Position: Clinical Research Coordinator III
Shift: Day Shift

Additional Responsibilities Include:

The day-to-day assignments for executing clinical trials will include study activation, process design and execution of study procedures as outlined by the study protocol (and related documents), screening potential participants, chart abstraction, survey administration, data reporting to sponsors and facilitation of monitoring visits and audits.  Will partner with regulatory and financial staff to support regulatory and patient billing compliance.

As a senior coordinator within the Clinical Research Center, this position may be called upon to help orient and mentor junior staff and to provide support to projects related to quality assurance and program development.

Education: BA/BS required with 4-5 years clinical research experience or MA/MS with 3 years clinical research experience.

Experience: Dependent on education as noted above. (Clinical research conducted while in the student environment may be considered on a case-by-case basis). Experience working in health care/health care setting required.

Licensures & Certifications: Successful completion of CITI Program and IATA training required within 3 months of hire.