Research Nurse - JobsRus.com Formerly CorTech
Richmond, VA
About the Job
JobsRUs.com is seeking to hire a Research Nurse for our client in Richmond, VA!
Benefits Available!
Weekly Pay!
Pay Rate - $38/hr
1st Shift: Monday-Friday, 5am-1pm position will required selected worker to work first half of contract at one client location and the other half at the second client location
Job Description
The Research Nurse is responsible for coordinating multiple research protocols and serving as a liaison with local investigators, clinical staff, and research personnel. Under direct supervision, this individual will mature in their understanding of research operations and regulations in order to achieve a strong fundamental understanding of human subject research.
Major Responsibilities
Duties include but are not limited to:
· 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.
· Complete study medication order forms accurately, when needed, and has physician or appropriate designee sign orders prior to medication administration
· Perform routine operational activities for multiple research protocols
· Liaise between site research personnel, industry sponsors, and Supervisor
· Collaborate closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable
· Coordinate protocol schedule of assessments from initial submission of feasibility until study closeout
· Coordinate submission and approval for the Site’s Facility Review Committee, if applicable
· Provide instruction on research protocols to appropriate staff, including interpretation of test results, observations, and related study data to physicians, nurses, and clinical staff
· Assess the patient and document findings at each clinic visit while on protocol
· Document all specific tasks required by the protocol (i.e. medication forms, quality of life questionnaires, neuro exams, vital signs sheets, times of lab draws, etc.)
· Complete the study medication order form accurately and have the physician or nurse practitioner sign orders prior to treatment
· Ensure that all medications are approved by the appropriate designee prior to initiating treatment or when changing medication regimens
· Accurately calculate and document the BSA, creatinine, STS calculation, or any other conversions needed, per protocol
· Document any interaction regarding the patient that occurs while the patient is enrolled on a protocol, including follow-up and survival (this includes home health intervention, pharmacies, and patient phone calls)
· Ensure that follow-up appointments, imaging, or any related procedures are scheduled correctly according to protocol requirements
· Accurately complete all data requests (including queries) and submit with source documentation within the timeframe specified in the SOP
· Generate and track drug shipments, device shipments, and supplies as needed
· Ensure timely and accurate data completion
· Track and report adverse events, serious adverse events, protocol waivers, deviations, and violations
· Communicate all protocol-related issues to appropriate study personnel or manager
· Re-consent patients in a timely manner and document process appropriately
Required Education and Experience
Associate's degree is required, bachelor's degree is preferred
1+ years of experience in patient care setting; proficient in various electronic applications, Microsoft Office, EDC, CTMS; knowledge of basic medical terminology
Or equivalent combination of education and/or experience
Licenses, Certifications, and Training
Registered Nurse - Currently licensed as a registered professional nurse in the state in which he or she practices, in accordance with law and regulation.
Knowledge, Skills, Abilities, and Behaviors
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
Working knowledge of medical and clinical research terminology
Demonstrate competency in EKG acquisition, phlebotomy, and other clinical tasks within nursing scope of work, as needed per licensure
Maintain HIPAA compliance knowledge and adhere to all HIPAA regulations, per HRI SOPs
Skills
Effective communication skills with internal and external customers
Strong organizational skills and time management with internal and external customers
Abilities
Interpersonal skills
Demonstrates a positive attitude in response to suggestions for improvement
Effectively prioritizes tasks and work assignments
Benefits Available!
Weekly Pay!
Pay Rate - $38/hr
1st Shift: Monday-Friday, 5am-1pm position will required selected worker to work first half of contract at one client location and the other half at the second client location
Job Description
The Research Nurse is responsible for coordinating multiple research protocols and serving as a liaison with local investigators, clinical staff, and research personnel. Under direct supervision, this individual will mature in their understanding of research operations and regulations in order to achieve a strong fundamental understanding of human subject research.
Major Responsibilities
Duties include but are not limited to:
· 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.
· Complete study medication order forms accurately, when needed, and has physician or appropriate designee sign orders prior to medication administration
· Perform routine operational activities for multiple research protocols
· Liaise between site research personnel, industry sponsors, and Supervisor
· Collaborate closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable
· Coordinate protocol schedule of assessments from initial submission of feasibility until study closeout
· Coordinate submission and approval for the Site’s Facility Review Committee, if applicable
· Provide instruction on research protocols to appropriate staff, including interpretation of test results, observations, and related study data to physicians, nurses, and clinical staff
· Assess the patient and document findings at each clinic visit while on protocol
· Document all specific tasks required by the protocol (i.e. medication forms, quality of life questionnaires, neuro exams, vital signs sheets, times of lab draws, etc.)
· Complete the study medication order form accurately and have the physician or nurse practitioner sign orders prior to treatment
· Ensure that all medications are approved by the appropriate designee prior to initiating treatment or when changing medication regimens
· Accurately calculate and document the BSA, creatinine, STS calculation, or any other conversions needed, per protocol
· Document any interaction regarding the patient that occurs while the patient is enrolled on a protocol, including follow-up and survival (this includes home health intervention, pharmacies, and patient phone calls)
· Ensure that follow-up appointments, imaging, or any related procedures are scheduled correctly according to protocol requirements
· Accurately complete all data requests (including queries) and submit with source documentation within the timeframe specified in the SOP
· Generate and track drug shipments, device shipments, and supplies as needed
· Ensure timely and accurate data completion
· Track and report adverse events, serious adverse events, protocol waivers, deviations, and violations
· Communicate all protocol-related issues to appropriate study personnel or manager
· Re-consent patients in a timely manner and document process appropriately
Required Education and Experience
Associate's degree is required, bachelor's degree is preferred
1+ years of experience in patient care setting; proficient in various electronic applications, Microsoft Office, EDC, CTMS; knowledge of basic medical terminology
Or equivalent combination of education and/or experience
Licenses, Certifications, and Training
Registered Nurse - Currently licensed as a registered professional nurse in the state in which he or she practices, in accordance with law and regulation.
Knowledge, Skills, Abilities, and Behaviors
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
Working knowledge of medical and clinical research terminology
Demonstrate competency in EKG acquisition, phlebotomy, and other clinical tasks within nursing scope of work, as needed per licensure
Maintain HIPAA compliance knowledge and adhere to all HIPAA regulations, per HRI SOPs
Skills
Effective communication skills with internal and external customers
Strong organizational skills and time management with internal and external customers
Abilities
Interpersonal skills
Demonstrates a positive attitude in response to suggestions for improvement
Effectively prioritizes tasks and work assignments
Source : JobsRus.com Formerly CorTech