Clin. Research Program Mgr

Description - External

Description:
Could you be our next Cardiovascular Clinical Research Program Manager with LIMR/Main Line Health?

Why work as a Clinical Research Program Manager with Main Line Health?

• Make an Impact! Be part of a cutting-edge cardiovascular clinical trials team! The Clinical Research Program Manager is integral to the clinical oversight for the cardiovascular trials program at the Lankenau Institute for Medical Research (LIMR) and the Main Line Health System. The Program Manager utilizes their clinical and managerial experience to promote clinical research activities, perform study coordinating services and provide guidance, oversight, and direction to the research team. Responsibilities include training, utilize various data collection systems in the conduct of drug and device clinical trials, review billing activity and monitoring reports, manage study distribution, meet research regulatory standards through the adherence of FDA guidelines and Good Clinical Practice, and promote patient safety.
• 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-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 240 hours of paid time off per year based on your Full-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 Program Manager
Shift: Day Shift

Education:  B.A/B.S. degree required, preferably in health sciences; Master's degree preferred.

Experience: 

1.     Minimum seven (7) years’ experience in clinical trials required; preferably cardiology and supervisory experience,

2.     Excellent communication and analytical skills; proficient in Microsoft office applications,

3.     Ability to manage various projects and teams,

4.     Knowledge of OHRP, FDA, HIPAA and GCP regulations,

5.     Familiarity with various electronic data collection systems.

Licensures & Certifications:  If applicable, current R.N. licensure in the Commonwealth of Pennsylvania. IATA & ACRP and/or SoCRA research certification required.