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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 Miami, FL.
· This position is to support a new clinical research program at a Hospital in Miami, FL. The research trials are specific to cardiac electrophysiology and experience in the specialty is preferred. If not possible, cardiology research experience preferred but must have research in clinical trials in alignment with the job description.
· 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 3 years of clinical research experience
· Must have at least 1 year of clinical trials specific to cardiac electrophysiology experience
· Computer skills with demonstrated abilities using web-based applications, electronic data capture, and MS Word or Excel
· 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
· Certified Clinical Research Coordinator (ACRP or CCRP) preferred
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 - FL
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 Miami, FL.
· This position is to support a new clinical research program at a Hospital in Miami, FL. The research trials are specific to cardiac electrophysiology and experience in the specialty is preferred. If not possible, cardiology research experience preferred but must have research in clinical trials in alignment with the job description.
· 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 3 years of clinical research experience
· Must have at least 1 year of clinical trials specific to cardiac electrophysiology experience
· Computer skills with demonstrated abilities using web-based applications, electronic data capture, and MS Word or Excel
· 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
· Certified Clinical Research Coordinator (ACRP or CCRP) preferred
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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