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Rezult Group
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Rezult Group continues to make great strides toward enhancing patient care through technology services nationwide. We are consistently looking for qualified professionals to join us in achieving success. Currently we are searching for a Clinical Research Coordinator to fulfill an immediate vacancy in Fort Worth, TX.
· The Clinical 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.
· Practice and adhere to the “Code of Conduct” philosophy and “Mission and Value Statement”.
· During your employment 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.
We are actively speaking with applicants that have a minimum of:
· Must have at least 1 year of clinical research experience in a hospital environment
· Must have clinical trials experience and able to handle multiple trials at one time
· Occasional Travel: The job may require travel from time- to-time, but not on a regular basis
· BA degree OR a Clinical Research Coordinator certification required
If your background, skills, and interest match the following; please apply online to ensure your credentials are reviewed by a skilled recruiter immediately. We look forward to working with you on this opportunity. For more information on Rezult Group and a list of additional job openings, please visit our website at www.rezultgroup.com.
Clinical Research Coordinator - TX
Job Description
Rezult Group continues to make great strides toward enhancing patient care through technology services nationwide. We are consistently looking for qualified professionals to join us in achieving success. Currently we are searching for a Clinical Research Coordinator to fulfill an immediate vacancy in Fort Worth, TX.
· The Clinical 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.
· Practice and adhere to the “Code of Conduct” philosophy and “Mission and Value Statement”.
· During your employment 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.
We are actively speaking with applicants that have a minimum of:
· Must have at least 1 year of clinical research experience in a hospital environment
· Must have clinical trials experience and able to handle multiple trials at one time
· Occasional Travel: The job may require travel from time- to-time, but not on a regular basis
· BA degree OR a Clinical Research Coordinator certification required
If your background, skills, and interest match the following; please apply online to ensure your credentials are reviewed by a skilled recruiter immediately. We look forward to working with you on this opportunity. For more information on Rezult Group and a list of additional job openings, please visit our website at www.rezultgroup.com.
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Ready to embark on an exciting career journey in Fort Worth, Texas? Explore our job listings in this vibrant city known as the 'City of Cowboys and Culture.' Fort Worth offers a perfect blend of rich Western heritage and modern amenities, making it an ideal destination for job seekers looking for growth opportunities and a high quality of life. From the iconic Fort Worth Stockyards to the world-renowned Kimbell Art Museum, there is something to enchant everyone here. Indulge in mouthwatering Tex-Mex cuisine, catch a show at the Bass Performance Hall, support the revered Fort Worth Symphony Orchestra, or cheer on the Dallas Cowboys at AT&T Stadium. Come discover why Fort Worth is the perfect place to take the next step in your career and experience its irresistible charm firsthand.
