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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 Nurse to fulfill an immediate contract vacancy in Richmond, VA.
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The Research Nurse coordinates multiple research protocols and serves as a liaison with investigators, clinical staff, and research personnel. Under supervision, this role develops a comprehensive understanding of research operations, regulations, and human subject research.
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Key Responsibilities:
·      Adhere to the organization’s Code of Conduct, Mission, and Value Statement.
·      Complete assigned training by deadlines.
·      Accurately prepare and obtain necessary approvals for study medication orders.
·      Perform routine activities for research protocols and coordinate across site personnel, sponsors, and supervisors.
·      Collaborate with site departments, including finance, hospital representatives, and the IRB.
·      Manage protocol schedules from feasibility to study closeout.
·      Provide protocol instructions to staff and interpret clinical data as needed.
·      Assess and document patient findings during clinic visits.
·      Ensure compliance with protocol-specific requirements, including medication approvals, data submissions, and follow-ups.
·      Track and report adverse events, protocol deviations, and violations.
·      Re-consent patients and document processes accurately.
·      Maintain timely and accurate data completion and communication.
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We are actively speaking with applicants that have a minimum of:
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·      1+ years in a patient care setting; proficiency in Microsoft Office, EDC, CTMS; and basic medical terminology.
·      Must have experience with high volume enrollment numbers in clinical trials.
·      Active Registered Nurse (RN) license in the practicing state.
·      Knowledge: Research protocols, ICH guidelines, CFR, HIPAA compliance, medical terminology.
·      Skills: Effective communication, organization, time management, and clinical task proficiency (e.g., EKG, phlebotomy).
·      Abilities: Interpersonal skills, positive attitude, and task prioritization.
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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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Clinical Research RN - VA
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 Nurse to fulfill an immediate contract vacancy in Richmond, VA.
Â
The Research Nurse coordinates multiple research protocols and serves as a liaison with investigators, clinical staff, and research personnel. Under supervision, this role develops a comprehensive understanding of research operations, regulations, and human subject research.
Â
Key Responsibilities:
·      Adhere to the organization’s Code of Conduct, Mission, and Value Statement.
·      Complete assigned training by deadlines.
·      Accurately prepare and obtain necessary approvals for study medication orders.
·      Perform routine activities for research protocols and coordinate across site personnel, sponsors, and supervisors.
·      Collaborate with site departments, including finance, hospital representatives, and the IRB.
·      Manage protocol schedules from feasibility to study closeout.
·      Provide protocol instructions to staff and interpret clinical data as needed.
·      Assess and document patient findings during clinic visits.
·      Ensure compliance with protocol-specific requirements, including medication approvals, data submissions, and follow-ups.
·      Track and report adverse events, protocol deviations, and violations.
·      Re-consent patients and document processes accurately.
·      Maintain timely and accurate data completion and communication.
Â
We are actively speaking with applicants that have a minimum of:
Â
·      1+ years in a patient care setting; proficiency in Microsoft Office, EDC, CTMS; and basic medical terminology.
·      Must have experience with high volume enrollment numbers in clinical trials.
·      Active Registered Nurse (RN) license in the practicing state.
·      Knowledge: Research protocols, ICH guidelines, CFR, HIPAA compliance, medical terminology.
·      Skills: Effective communication, organization, time management, and clinical task proficiency (e.g., EKG, phlebotomy).
·      Abilities: Interpersonal skills, positive attitude, and task prioritization.
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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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