Clinical Research Coord II

About the Role

The Cardiovascular Clinical Research Department is looking for an experienced Coordinator Research Coordinator to join our team. The Clinical Research Coordinator will manage a variety of device trials and support Phase II-IV drug studies. Daily tasks are conducted on site at the Main Line Health Hospitals and may include the oversight and coordination of a variety of clinical studies, executing study procedures as outlined by the study protocol (and related documents). The CRC will require impeccable attention to detail, sound judgment, and a high level of knowledge of protocol requirements and medical terminology. This individual will work under physician investigator guidance and with our clinical team and a variety of hospital individuals, patients and study sponsors. Collaboration with senior clinical research staff and Clinical Research Center leadership is crucial for the successful candidate.

Responsibilities

• Manage a variety of device trials
• Support Phase II-IV drug studies
• Oversee and coordinate a variety of clinical studies
• Execute study procedures as outlined by the study protocol and related documents
• Work under physician investigator guidance
• Collaborate with clinical team, hospital individuals, patients, and study sponsors
• Collaborate with senior clinical research staff and Clinical Research Center leadership

Qualifications

• BA/BS required in a science focused major
• Hospital or clinical setting experience of 1-3+ years, preferably related to cardiology, cardiac surgery and/or vascular surgery
• Field related experience in a related medical area considered
• Clinical research conducted while in the student environment and past positions may be considered on a case-by-case basis
• Strong written and verbal skills in the English language

Skills

• Impeccable attention to detail
• Sound judgment
• High level of knowledge of protocol requirements and medical terminology
• Proficiency in utilizing multiple e-based tools: Office365/SharePoint, OneDrive and Microsoft Office tools, navigating websites
• Utilization of complex databases, electronic health records (EHR) systems and web-based data collection tools (i.e. REDCAP)

Licensures/Certifications

• Successful completion of CITI Program and IATA training required within 3 months of hire
• ACRP research certification encouraged

Schedule

8am-4:30pm and variable, Monday-Friday. Flexibility required to manage study coverage and responsibilities.

Location

Clinical research program focused at Lankenau Medical Center and Bryn Mawr Hospital. May expand to Riddle Hospital and Paoli Hospital. Requires the ability to travel periodically between health system hospitals.

Benefits

• Tuition Reimbursement up to $6,000 per year based upon Full or Part Time status
• Up to 160 hours of paid time off per year based upon Full or Part Time status
• Employee discounts to various activities, services, and vendors
• Employee parking is always free