Clinical Research Coordinator job in Tomball, TX
Tomball, TX CorTech LLC
| Job Ref: | 369226 |
| Employer: |
CorTech LLC |
| Job Type: | Contract |
| Salary and Benefits: | 35.86/Per Hour |
| Remote: | No |
Location |
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| City: | Tomball, TX |
| Post Code: | 77375 |
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Description |
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JobsRUs.com is seeking to hire a Clinical Research Coordinator for our client in Tomball, TX! Benefits Available! Weekly Pay! Pay Rate - $35.86/hr 1st Shift: Monday-Friday, 8am-5pm 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. This role is a non-clinical CRC position for our hospitals, meaning you'll be traveling between two locations. This position will be working on a single trial called the PREPARE trial for pre-eclampsia screening. This role would be screening and enrolling patients for the single study between both locations. This is a high enrolling trial, so organization and clinical research project management will be critical to the success of this role. Major Responsibilities ? 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 relevant experience, or equivalent combination of education and experience. Preferred Certifications Clinical Research Coordinator certification is preferred. Knowledge, Skills, and Abilities 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: (369226)
less than 2 minutes ago
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