Sr Clinical Research Associate

St. Jude Children's Research Hospital • Memphis, TN

3d • $78,000 - $139,360

About The Position

There’s a reason St. Jude Children’s Research Hospital is consistently ranked on Glassdoor’s “Best Places to Work” list. Actually, there are more than 6,500 reasons. At our world-class pediatric research hospital, every one of our 6,500 professionals shares our commitment to making a difference in the lives of the children we serve. There’s a unique bond when you are part of a team that will stop at nothing to advance the treatments and cures of pediatric catastrophic diseases. The result is a collaborative, positive environment where all employees, regardless of their role, receive the resources, support, and encouragement to advance and grow their careers. The Sr Clinical Research Associate is responsible for performing data abstraction, collection, and entry to support clinical research. Develops, maintains, and/or monitors case report forms. Ensures compliance with prescribed interventions and evaluations of the assigned protocol(s). Provides data and reports to the collaborating research organization or study sponsor.

Requirements

• Bachelor's degree in relevant area required.
• Minimum Requirement: 4+ years of experience in carrying out research preferably in healthcare settings.
• Experience managing cross-functional communication, including liaison between site and study teams.
• Experience with documentation and tracking systems/processes.
• Proven performance in earlier role.

Nice To Haves

• Master's degree preferred.
• Experience Exception: Master's degree and 2+ years of experience.
• Experience with study start up preferred.
• Experience with regulatory processes during study start up preferred.

Responsibilities

• Support project management (lead/monitor planning and delivery) for institutional as well as St. Jude sponsored, multi-center trials, including regulatory, financial, and administrative aspects of the study.
• Act as site study coordinator for complex, large multi-site and/or multidisciplinary clinical trials.
• Maintain and share essential study documents (e.g., investigator files, case report forms) as required.
• Assist with protocol submissions (internally sponsored and/or externally sponsored) for review by federal or institutional committees (e.g., CPSRMC and IRB) as applicable.
• Assist in the development of ongoing review of departmental/divisional standard operating procedures. and ensure compliance in execution of assigned tasks.
• Oversee quality of data abstraction, collection, and entry to support clinical research of study team members. (As applicable)
• Provide patient care, education, and management (e.g., routine test conduct; assistance in clinical procedures; medication instruction, monitoring, and documentation; patient care coordination; education on protocol activities).
• Perform other duties as assigned to meet the goals and objectives of the department and institution.
• Maintains regular and predictable attendance.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees