Clinical Research Coordinator job in Humble, TX
Humble, TX CorTech LLC
| Job Ref: | 366555 |
| Employer: |
CorTech LLC |
| Job Type: | Contract |
| Salary and Benefits: | 35.86/Per Hour |
| Remote: | No |
Location |
|
| City: | Humble, TX |
| Post Code: | 77339 |
| Map: |
|
Description |
|
|
JobsRUs.com. is seeking to hire a Clinical Research Coordinator for our client in Humble, TX! Benefits Available! Weekly Pay! $35.86/Hour Shift Details: 1st shift Working Days: Monday - Friday Day starts at: 7:00AM Day Ends at: 4:00PM DESCRIPTION: Position Summary: 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: 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 or 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 or 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 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 Education AND Experience: Bachelor?s Degree 1+ years of relevant experience Or equivalent combination of education or experience Licenses, Certifications, & Training: Certified Clinical Research Coordinator Knowledge, Skills, Abilities, Behaviors: 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 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 An underlying, enduring trait useful for performing duties Clinical Competencies: This role may require competency in performing clinical tasks, including ECG, phlebotomy, and the process of handling, centrifuging, storing and shipping of specimens. Demonstrating the ability to perform core competencies will be evaluated, at a minimum, annually. Training or certification will be provided when mandatory, per protocol. | |
ref: (366555)
less than 2 minutes ago
Back to search results