Clinical Research Coord I

Description:
Could you be our next Clinical Research Coordinator at Bryn Mawr Hospital?

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

* Make an Impact! The Clinical Research Coordinator I will manage a variety of clinical research projects with oversight by senior staff and investigators, for the Oncology Clinical Research Program. The day-to-day assignments for executing clinical trials will include the execution of study procedures as outlined by the study protocol (and related documents), screening medical records for eligible research patients, scheduling appointments, collecting and entering data into trial systems in collaboration with junior staff, and collaborating with senior staff and investigators to manage source data and reporting requirements. The CRCI will require an impeccable attention to detail, sound judgment, and a high level of knowledge of protocol requirements and medical terminology. This role is Patient Facing, interacting with Oncology patients in the hospital and clinic setting. This individual will work under direct supervision and instruction

• 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 200 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
Shift: 8am-4:30p, Monday-Friday

Experience:

1-2 years clinical research experience. (Clinical research conducted while in the student environment may be considered on a case-by-case basis. Experience working in a healthcare setting preferred.

Education:
BA/BS required.

Licensures/Certifications:

Successful completion of CITI Program and IATA training required within 3 months of hire. ACRP research certification highly encouraged within 1 year of hire.