Clinical Research Coordinator II job in Nashville, TN
Vacancy has expired
Nashville, TN CorTech LLC
| Job Ref: | 347021 |
| Employer: |
CorTech LLC |
| Job Type: | Contract |
| Salary and Benefits: | 34.48/Per Hour |
| Remote: | No |
Location |
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| City: | Nashville, TN |
| Post Code: | 37203 |
| Map: |
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Description |
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CorTech is seeking to hire a Clinical Research Coordinator II for our client in Nashville, TN! Benefits Available! Weekly Pay! $34.48/Hour Position Summary The Clinical Research Coordinator II 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. This individual seeks to demonstrate a moderate to advanced level of independence when performing research coordination duties and can apply skills to a broad range of study types. Major Responsibilities: Duties include but are not limited to: Practices and adheres to the ?Code of Conduct? philosophy and ?Mission and Value Statement? Ability to satisfy all responsibilities of the CRC Level I Job Description 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 Review the study design and inclusion/exclusion criteria with physician and patient Ensure the protection of study patients by verifying informed consent procedures and adhering to protocol requirements Ensure the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review; monitors data for missing or implausible data 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 data capture systems Generate and track drug shipments, device shipments, and supplies as needed Ensure timely and accurate data completion Track and report adverse events, serious adverse events, protocol waivers, deviations, and violations Communicate all protocol-related issues to appropriate study personnel or manager Attend study specific on-site meetings, investigator meetings, conference calls and monthly CRC meetings, as required Review and respond to any monitoring and auditing findings Assist in providing coverage for satellite clinic sites as necessary 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 document 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 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 Required Degree Preferred 1+ years of relevant experience Required 3+ years of relevant experience Preferred Or equivalent combination of education and/or experience Licenses, Certifications, & Training: Certified Clinical Research Coordinator (ACRP or CCRP) Preferred 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 Abilities: An underlying, enduring trait useful for performing duties Interpersonal skills Self-motivated Meticulous eye for detail | |
ref: (347021)
985 days ago
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