Sr. Clinical Research Coordinator job in Brentwood, TN
Vacancy has expired
Brentwood, TN CorTech LLC
| Job Ref: | 367384 |
| Employer: |
CorTech LLC |
| Job Type: | Contract |
| Salary and Benefits: | 44.57/Per Hour |
| Remote: | No |
Location |
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| City: | Brentwood, TN |
| Post Code: | 37027 |
| Map: |
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Description |
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JobsRUs.com. is seeking to hire a Sr. Clinical Research Coordinator for our client in Brentwood, TN! Benefits Available! Weekly Pay! $44.57/Hour Shift Details: 1st shift Working Days : Monday- Friday Day Starts at: 08:00AM Day End at : 05:00PM JOB DESCRIPTION: 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. Major Responsibilities: Duties include but are not limited to: Practices and adheres to the ?Code of Conduct? philosophy and ?Mission and Value Statement? Demonstrate ability to fulfill responsibilities and duties of the CRC Level I and II Assist with training CRC Level I and II personnel Act as a role model to peers Clinical Research Operations 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 (i.e. medication forms, quality of life questionnaires, neuro exams, vital signs sheets, times of lab draws, etc.) Accurately perform/calculate and documents the BSA, mRS, NIHSS, STS risk score, or any other approved CRC task, as needed per protocol Document all patient, staff, and sponsor correspondence, including follow-up encounters, adverse events, interventions, pharmacy dispensations, and patient phone calls Ensure follow-up appointments, imaging, or any related procedures are scheduled correctly according to protocol requirements Accurately complete all data requests (including queries) 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 Site Development Work with site personnel and local investigators to assess site feasibility and performance Regularly meet with physicians and administrators, when applicable, to assess study performance and investigator satisfaction Collaborate with other departments (non-invasive, finance, laboratory, etc.) to develop and implement processes in support of the research activities Assist with providing a research update during Site Administrative meetings (Section meetings, Site Service Line meetings, etc.) Able to guide research team members on the management of non-compliant data and/or study activities Reporting and Analysis Monitor patient enrollment at the site through weekly reports, and reports results to Supervisor Facilitate continuing education and training to investigators, as applicable Enter any content that you want to repeat, including other content controls. You can also insert this control around table rows in order to repeat parts of a table. Education & Experience: Bachelor?s Degree 1+ years of relevant experience Or equivalent combination of education and/or experience Licenses, Certifications, & Training: Certified Clinical Research Coordinator (ACRP or CCRP) Knowledge, Skills, Abilities, Behaviors: Knowledge: Knowledge of organizational policies, standard operating procedures, and systems Demonstrate understanding and application of ICH guidelines and the Code of Federal Regulations within the clinical research environment. Fundamental understanding of medical and research operations terminology Recognize circumstances requiring prompt escalation to PI, IRB, and/or Supervisor Skills: The proficiency to perform a certain task Effective communication skills Strong organizational skills and time management Basic clinical trial procedures, including ECG acquisition, phlebotomy, and specimen processing, handling, storing, and shipping. Effective interfacing with site stakeholders | |
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