Clinical Research Coordinator job in New Port Richey, FL
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New Port Richey, FL CorTech LLC
| Job Ref: | 367023 |
| Employer: |
CorTech LLC |
| Job Type: | Contract |
| Salary and Benefits: | 35.86/Per Hour |
| Remote: | No |
Location |
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| City: | New Port Richey, FL |
| Post Code: | 34655 |
| Map: |
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Description |
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JobsRUs.com is seeking to hire a Clinical Research Coordinator for our client in Trinity, FL! Benefits Available! Weekly Pay! 6 Month Contract Pay Rate - $35.86/hr 1st Shift: Monday-Friday, 7am-4pm Job Description The Research Coordinator position is responsible for Coordinating multiple research protocols and serving as a liaison with local investigators and Sponsors. Under direct supervision, this individual will mature in their understanding of research operations and regulations in order to achieve a fundamental understanding of human subject research. Major Responsibilities Duties include but not limited to: · Practice and adhere to the ?Code of Conduct? philosophy and ?Mission and Value Statement? · During your employment with HRI you will be routinely assigned training requirements. You are expected to complete any training assignments by the due date. · Performs routine operational activities for multiple research protocols · Liaise between site research personnel, industry sponsors, and Supervisor · Collaborates closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable · Coordinates schedule of assessments from initial submission of feasibility until study closeout · Reviews the study design and inclusion/exclusion criteria with physician and patient · Ensures the protection of study patients by verifying informed consent procedures and adhering to protocol requirements · Ensures 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 · Creates study specific tools for source documentation when not provided by sponsor · Collects, completes, and enters data into study specific case report forms or electronic data capture systems · Generates and tracks drug shipments, device shipments, and supplies as needed · Ensures timely and accurate data completion · Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations · Communicates all protocol-related issues to appropriate study personnel or manager · Attends study specific on-site meetings, investigator meetings, conference calls and monthly CRC meetings, as required · Reviews and responds to any monitoring and auditing findings Required Education and Experience Bachelors degree in a related field 1+ years of related experience Clinical Research Coordinator Certification preferred Knowledge, Skills, Abilities, and Behaviors Knowledge: · Knowledge of organizational policies, standard operating procedures, and systems · Emerging understanding and application of ICH guidelines and the Code of Federal Regulations within the clinical research environment. · Basic understanding of medical terminology 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 Abilities: An underlying, enduring trait useful for performing duties · Interpersonal skills · Self-motivated · Meticulous eye for detail | |
ref: (367023)
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