Clinical Research Nurse Cover Letter

Please consider me for the clinical research nurse opportunity. I am including my resume that lists my qualifications and experience.

In the previous role, I was responsible for education to patients on compliance, possible side effects, drug interactions and the importance of contacting the coordinator.

Please consider my experience and qualifications for this position:

• COMP - Successfully uses multiple software programs independently
• COW - Communicates effectively one-to-one, in small groups and in public speaking contexts
• ENI - Follows through on commitments
• HEALTH – Integrates health and safety precautions into daily activities
• QUALITY – Striving for excellence with our work processes and outcomes, honoring University policies and regulatory requirements
• Master of Science in Nursing with oncology specialty
• Investigational agents, coordination of clinical research and data
• Exercise discretion when making judgments and to determine proper course of action while following established standards

I would like to submit my application for the clinical research nurse opening. Please accept this letter and the attached resume.

Previously, I was responsible for direct care to research patients, including drug administration, lab draws, coordination of appointments, follow-up and management of side effects, identification of home care needs.

Please consider my experience and qualifications for this position:

• Oversee ongoing protocol operations to ensure study compliance and troubleshoot possible protocol violations
• Work with the participating Branches within CCR to maintain protocol compliance and adherence
• Collegiality - Helpful, respectful, approachable
• Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP) certification preferred
• Participates in research participant recruitment
• Obtains all appropriate outside records to support prior history, treatments, and eligibility and sends to NIH Clinical Center Medical Records Department
• Contributes to the development of case report forms
• Develops study-specific materials for research participant education

Please consider me for the clinical research nurse opportunity. I am including my resume that lists my qualifications and experience.

In the previous role, I was responsible for information and advice regarding drug interactions, side effects, dosage and proper medication storage.

Please consider my experience and qualifications for this position:

• Knowledge of Concepts, Procedures, and Techniques
• Proficiency in Microsoft office, excel and access
• Current certification, such as Certified Clinical Research Coordinator (CCRC)
• Minimum six months of clinical experience
• Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred
• Assist the Principal Investigator (PI) in data collection (including patient specimens) and data analysis
• Coordinate Clinical Trial Agreement requirements with applicable Clinical Research Oversight Managers (e.g., safety reporting requirements) and data management if data is to be provided to third party at end of trial
• Assist in managing patient files, copying and organizing research data

I would like to submit my application for the clinical research nurse opening. Please accept this letter and the attached resume.

Previously, I was responsible for patient education and medical information to study participants to ensure understanding of proper medication dosage, administration, and disease treatment.

My experience is an excellent fit for the list of requirements in this job:

• Recognize and support the needs of data integrity and retrieval, and interpret needs appropriately for PIs, patients and other staff members
• Ensure scientific quality and human subject’s protection
• Collect and interpret data as specified by the investigators in support of the clinical trial including drug administration, toxicity, laboratory parameters and response interpretation
• Coordinate and review daily operations and logistics
• Ensure the communication of study changes to all care givers
• Interface with the Protocol Support Office
• Manage dose modifications and/or other modifications of the treatment regimen made in response to toxicity, pharmacokinetics, and tissue studies
• Order labs, x-rays and other diagnostic procedures prescribed by the protocol and/or clinically indicated

I would like to submit my application for the clinical research nurse opening. Please accept this letter and the attached resume.

In my previous role, I was responsible for direct care to research subjects, including drug administration, lab draws, coordination of appointments, follow-up and management of side effects under the guidance of PI, etc.

My experience is an excellent fit for the list of requirements in this job:

• Participates in the setup and management of study-specific databases
• Educates the research participant and family on participant’s current clinical condition and/or disease process
• Monitors research participant and reports potential adverse events to a member of the research team
• Records research data (vital signs, administration of a research compound, participant responses, ) in approved source document (medical record, case report forms)
• Participates in the identification and reporting of research trends
• Collaborates with Protocol Navigator to maintain accurate and complete regulatory binder
• Participates in Institutional Review Board (IRB) submissions
• Participates in quality assurance initiatives (responds to queries, assists with attribution of adverse events, attends weekly meeting with data management staff, and responds to monitoring and auditing reports)