Clinical Research Coordinator Position Available In Davidson, Tennessee

Tallo's Job Summary: We are seeking a Clinical Research Coordinator for our client company. This role involves performing routine operational activities for multiple research protocols, liaising between site research personnel and industry sponsors, as well as collaborating with various site departments to ensure successful coordination of the research studies. The ideal candidate should be proficient in data collection and entry, possess strong collaboration and communication skills, and be detail-oriented to ensure data integrity and compliance.

Company:
Medix
Salary:
JobFull-timeOnsite

Job Description

You are applying for a position through Medix, a staffing agency. The actual posting represents a position at one of our clients. Job Summary We are seeking a Clinical Research Coordinator for our client company. This role involves performing routine operational activities for multiple research protocols, liaising between site research personnel and industry sponsors, as well as collaborating with various site departments to ensure successful coordination of the research studies. Key Responsibilities Practice and adhere to the “Code of Conduct” philosophy and “Mission and Value Statement”. Complete training assignments by due dates. Perform routine operational activities for multiple research protocols. Liaise between site research personnel, industry sponsors, and Supervisor. Collaborate closely with site departments, finance, hospital administrative representatives, and local IRB if applicable. Coordinate schedule of assessments from submission of feasibility until study closeout. Review study design and inclusion/exclusion criteria with physicians and patients. Verify informed consent procedures to ensure protection of study patients. Ensure integrity of data submitted on Case Report Forms through careful document review. Create study specific tools for source documentation when not provided by sponsor. Collect, complete, and enter data into study specific case report forms or electronic systems. Generate and track drug, device shipments, and supplies as needed. Ensure timely and accurate data completion. Track and report adverse events, protocol waivers, deviations, and violations. Communicate all protocol-related issues to relevant study personnel or manager. Attend study specific meetings and conference calls as required. Review and respond to monitoring and auditing findings. Skills Proficient in data collection and entry. Strong collaboration and communication skills. Detail-oriented with the ability to ensure data integrity and compliance.

Medix Overview:

With over 20 years of experience connecting organizations with highly qualified professionals, Medix is a leading provider of workforce solutions for clients and candidates across the healthcare, scientific, technology, and government industries. Through our core purpose of positively impacting lives, we’re dedicated to creating opportunities for job seekers at some of the nation’s top companies. As an award-winning career partner, Medix is committed to helping talent find fulfilling and meaningful work because our mission is to help you achieve yours.

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