Senior Clinical Research Coordinator

HCA Healthcare • Dallas, TX, United States • $200k - $250k / year • 3w ago

Location: Nashville, Tennessee

HCA Healthcare Senior Clinical Research Coordinator

*This position will sit on-site at our Medical City Dallas location in Dallas, TX

Introduction

Are you looking for a work environment where diversity and inclusion thrive? Submit your application for our Senior Clinical Research Coordinator opening with HCA Healthcare today and find out what it truly means to be a part of the HCA Healthcare team.

We are seeking a Senior Clinical Research Coordinator for our team to ensure that we continue to provide all patients with high quality, efficient care. Did you get into our industry for these reasons? We are an amazing team that works hard to support each other and are seeking a phenomenal addition like you who feels patient care is as meaningful as we do. We want you to apply!

Job Summary and Qualifications

The Senior Clinical Research Coordinator is responsible for coordinating multiple research protocols; serving as a liaison with local investigators and research personnel; and acting as a central resource for assigned research projects. The individual in this role offers a significant contribution to the development of processes, tools, and training necessary to maintain site compliance and patient safety.

What qualifications you will need:

2-3 years of Clinical Research Coordinator experience required
Bachelor’s Degree required
Certified Clinical Research Coordinator (ACRP or CCRP) preferred
Knowledge of federal regulations, good clinical practices (GCP), and medical & research terminology
Computer skills, including use of clinical trial database, electronic data capture, and MS Word or Excel
The ability to communicate and work effectively with a diverse team of professionals
The ability to work independently in a fast pace environment with minimal supervision at off-site facilities

What you will do in this role:

Perform routine operational activities for multiple research protocols
Liaise between site research personnel, industry sponsors, and Supervisor
Collaborate closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable
Coordinate schedule of assessments from initial submission of feasibility until study closeout
Coordinate submission and approval for the Site’s Facility Review Committee, if applicable
Provide awareness of research protocols to appropriate site-level personnel, including physicians, nurses, clinical staff, and administrators
Document all specific tasks required by the protocol
Accurately perform/calculate and document required tasks as needed per protocol
Document all patient, staff, and sponsor correspondence
Ensure follow-up appointments, imaging, or any related procedures are scheduled correctly according to protocol requirements
Accurately complete all data requests and submit with source documentation within the timeframe specified in the SOP
Re-consent patients in a timely manner and document process appropriately
Support study team in mitigating risks and optimizing site compliance
Work with site personnel and local investigators to assess site feasibility and performance
Regularly meet with physicians and administrators to assess study performance and investigator satisfaction
Collaborate with other departments to develop and implement processes in support of the research activities
Assist with providing a research update during Site Administrative meetings
Able to guide research team members on the management of non-compliant data and/or study activities
Monitor patient enrollment at the site through weekly reports, and report results to Supervisor
Facilitate continuing education and training to investigators, as applicable

If you find this opportunity compelling, we encourage you to apply for our Senior Clinical Research Coordinator opening. We promptly review all applications. Highly qualified candidates will be directly contacted by a member of our team. We are interviewing apply today!

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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