Clinical Research Nurse (Temporary Assignment)

At Cutera, a Clinical Research Nurse is integral in providing patient care and supporting clinical research at our Clinical Research Center. Key responsibilities include administering aesthetic treatments, recruiting and enrolling study participants, ensuring informed consent is obtained, and documenting patient progress and outcomes. You will also collaborate with physicians and clinical staff to ensure that all research activities comply with established regulatory standards.

To qualify for the Clinical Research Nurse role at Cutera, you need to be a Registered Nurse (RN) with an active license. A minimum of three years of clinical experience, preferably in dermatology or aesthetics, is required. Additionally, experience in a clinical research setting is preferred, along with a strong knowledge of Good Clinical Practices (GCP) and FDA regulations. Excellent communication and organizational skills are essential for this position.

As a Clinical Research Nurse at Cutera, you can expect to work on-site five days a week for up to 30 hours per week. Daily tasks may include administering treatments, monitoring patient progress, collaborating with other clinical team members, and maintaining accurate patient records. Each day provides the opportunity to engage with patients and contribute to innovative clinical research in a fast-paced, high-tech environment.

In your role as a Clinical Research Nurse at Cutera, you will administer laser and aesthetic treatments in accordance with approved clinical protocols. This includes treatments that enhance skin appearance, such as addressing superficial benign vascular lesions, improving skin laxity, and body contouring. Training will be provided to ensure you are comfortable using Cutera's advanced devices.

While prior experience using Cutera devices is preferred for the Clinical Research Nurse position, it is not mandatory. What’s most important is that you have a solid background in clinical nursing and a willingness to learn and adapt quickly to new technologies. Cutera is committed to providing the necessary training to ensure you're fully equipped to succeed in this role.

To ensure compliance with clinical research protocols, I familiarize myself with all aspects of the study design and regulatory requirements. I maintain detailed and accurate documentation, regularly audit my records for compliance, and participate in ongoing training to stay updated on GCP and FDA regulations.

In my previous positions, I consistently worked in busy clinical settings where I managed multiple tasks, including patient care and administrative duties. I prioritize tasks effectively and communicate efficiently with team members to ensure that all patient needs are met without compromising quality.

For patient education, I focus on clear communication, using layman's terms to explain procedures, risks, and benefits. I encourage questions and ensure they feel comfortable with the information provided before obtaining informed consent, emphasizing the importance of understanding their decision.

In a previous role, I encountered a patient who was anxious about their treatment. I listened actively to their concerns, validated their feelings, and took the time to walk them through the process step-by-step, which helped them feel more at ease and created a positive experience.

I adhere to strict protocols for documentation, ensuring all patient interactions, treatment details, and research findings are recorded accurately and promptly. I double-check entries for completeness and accuracy and routinely review documentation with team members to prevent any discrepancies.

GCP refers to the ethical and scientific quality standards for designing, conducting, and reporting clinical studies involving human subjects. My understanding of GCP includes the importance of protecting study participants' rights, ensuring data integrity, and adhering to regulatory requirements throughout the research process.

To stay current, I regularly attend workshops, webinars, and training sessions focused on clinical research developments and regulations. I also subscribe to relevant journals and participate in professional organizations to network with other experts in the clinical research field.

I am deeply motivated by the prospect of improving patient outcomes and contributing to advancements in medical aesthetics. Being a part of research that has the potential to enhance lives drives my passion for patient care and research.

I prioritize tasks by assessing the urgency and impact of each responsibility. I maintain a running list of tasks, ensuring that patient safety and care remain my top priority while also being flexible to adjust my focus as new issues arise.

I have extensive experience collaborating with various stakeholders, including physicians, coordinators, and administrative staff. I believe that effective communication and respect for each team member's expertise are crucial for achieving successful outcomes in clinical research.