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Clinical Research Coordinator

Company Description

Cutera is a leading global aesthetics device company with a comprehensive product portfolio and a global distribution footprint. We are a fast-paced, high-tech medical device company looking for the right person to help grow our business and reap the rewards of doing it! We hire the best people and provide them the best comp and benefits to help improve their lives. Read more at www.cutera.com

Our Company’s technology enables physicians to provide advanced solutions for a broad range of medical aesthetic applications including improving the skin’s appearance through the treatment of superficial benign vascular and pigmented lesions, hair removal, improvement in skin laxity and wrinkles, and body contouring and sculpting.

Job Description

Position Summary:

We are seeking a detail-oriented and organized Clinical Research Coordinator to support patient recruitment, scheduling, data collection and entry, supply and equipment tracking, regulatory binder maintenance and administrative tasks within our Clinical Research Center. This role involves coordinating patient treatment visits, maintaining accurate records, and ensuring seamless communication between study sites, physicians, patients and research teams. The ideal candidate will have prior experience in clinical research, strong interpersonal skills, proficiency in Microsoft Office applications, and the ability to manage multiple tasks efficiently. Experience in Photoshop is a plus.

Please note this is an hourly, part-time position and will work on-site 5 days per week in Brisbane, CA.

Duties & Responsibilities:

  • Coordinate and track participant recruitment, screening, and enrollment.
  • Schedule patient treatment visits and follow-up appointments.
  • Communicate patient visit schedules through the appropriate channels including the Clinical Research Center Group, Clinical Research Department, and individual study sites.
  • Take before and after photograph of all patients at each treatment, as well as follow-up appointments for CRC patients and other San Francisco Bay Area study-site locations.
  • Greets patients and visitors in a prompt, professional, and respectful manner.
  • Patient Check-In: verifies and/or updates patient paperwork at every visit.
  • Organize study patients before and after photos for physician review.
  • Support collection, entry, and management of patient and/or study data into case report forms and/or Company’s database.
  • Accurately order, track and manage research and clinic supplies and equipment.
  • Maintaining study regulatory binders, ensuring all study documents are accurate, complete and up-to-date.
  • Other projects may include administrative tasks such as data consolidation, filing and other light office tasks.
  • Other duties as assigned.

Qualifications

Minimum Requirements & Qualifications: 

  • AA/AS degree or equivalent with one or more years of related administrative experience in patient scheduling, coordination, and clinical research.
  • Familiarity with clinical trials processes, good clinical practice (GCP) standards and ethical considerations in clinical research.
  • Proficiency in Microsoft software applications (Power Point, Word, Excel, Outlook) required.
  • Must be able to communicate effectively and collaboratively with Clinical team.
  • Excellent communication and interpersonal skills required.
  • Careful attention to detail and ability to work independently and multitask.
  • Excellent organizational skills and ability to prioritize a variety of tasks, foresee needs and initiate improvements.
  • Understanding of basic medical terminology.
  • Experience in Photoshop software is preferred.

Additional Information

Cutera expects to reasonably pay in the range listed below for this position based on the city and state listed in the job posting. The actual compensation is influenced by a wide array of factors, including but not limited to skill set, level of experience, education, and candidate residence if the position is remote or field-based.

Hourly rate:  $30 - $37 per hour

All your information will be kept confidential according to EEO guidelines.

If you are ready to become part of our spectacular, growing, and FUN company, then apply today!

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, perform essential job functions, and receive other benefits and privileges of employment. Please contact us to request accommodation.

Applicants responding to this posting must be able to provide proof of eligibility to work in the United States. Competitive salary, benefits, ESPP and stock options. Cutera is an Equal Employment Opportunity Employer.

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CEO of Cutera
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$62400K
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What You Should Know About Clinical Research Coordinator, Cutera

At Cutera, we're looking for a passionate and detail-oriented Clinical Research Coordinator to join our vibrant team in Brisbane, CA! If you're someone who thrives in a fast-paced environment and loves supporting clinical research, this could be the perfect role for you. As a Clinical Research Coordinator, your main duties will include coordinating patient recruitment efforts, scheduling appointments, and managing data collection and entry for our Clinical Research Center. You’ll actively communicate with study sites and ensure that patients feel welcomed and informed throughout their visits. With your strong organizational and interpersonal skills, you'll track participant recruitment efficiently and maintain accurate records, helping ensure every aspect of our clinical trials runs smoothly. Prior experience in clinical research will be a big plus, and being proficient in Microsoft Office will make your transition seamless. This is a part-time role that requires you on-site five days a week, where you'll also have the opportunity to utilize your skills in taking before and after photos for our patients. If you're ready to enhance your career while working alongside a dynamic team dedicated to revolutionizing medical aesthetics, we encourage you to apply and see how you can play a vital role in our mission at Cutera!

Frequently Asked Questions (FAQs) for Clinical Research Coordinator Role at Cutera
What responsibilities does a Clinical Research Coordinator at Cutera have?

At Cutera, a Clinical Research Coordinator plays a vital role in the success of clinical trials. This individual is responsible for coordinating participant recruitment, scheduling appointments for treatments, and maintaining accurate data collection and entry. Furthermore, they manage communication between patients, study sites, and clinical teams, ensuring a smooth and professional experience for all involved.

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What qualifications are necessary for the Clinical Research Coordinator position at Cutera?

To be considered for the Clinical Research Coordinator role at Cutera, candidates should have an AA/AS degree or equivalent experience, along with at least one year of relevant administrative experience in patient scheduling and clinical research. Familiarity with clinical trial processes and ethical standards in research is essential, and proficiency in Microsoft Office applications is required for effective communication and data management.

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What skills are essential for a Clinical Research Coordinator at Cutera?

Essential skills for a Clinical Research Coordinator at Cutera include excellent communication and interpersonal abilities to engage with patients and the clinical team, keen attention to detail for maintaining accurate records, and solid organizational skills to multitask effectively. Additionally, having a basic understanding of medical terminology and experience with Photoshop is advantageous.

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How does Cutera support its employees in professional growth as Clinical Research Coordinators?

Cutera places a strong emphasis on employee development and growth. As a Clinical Research Coordinator, you will receive on-the-job training, gain valuable experience in clinical research, and work alongside skilled professionals in the field. We encourage our employees to pursue further education and training to enhance their skills and advance in their careers.

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What is the work environment like for a Clinical Research Coordinator at Cutera?

The work environment for a Clinical Research Coordinator at Cutera is collaborative and filled with energy. You will be part of a supportive team focused on high-quality patient care and innovative research. The role requires being on-site five days a week in Brisbane, CA, where you can expect a busy, yet rewarding atmosphere surrounded by professionals dedicated to transforming medical aesthetics.

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Common Interview Questions for Clinical Research Coordinator
Can you describe your experience with coordinating clinical trials?

When answering this question, you should highlight specific experiences where you managed patient recruitment, scheduled appointments, or maintained regulatory documents. Discuss how you ensured compliance with GCP standards and how your organizational skills contributed to the success of previous trials.

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How do you prioritize tasks as a Clinical Research Coordinator?

In response, you should demonstrate your ability to multitask by describing a time when you successfully managed multiple responsibilities. Explain how you evaluate urgency, delegate when necessary, and use tools like calendars or project management software to keep activities on track.

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What strategies do you use to effectively communicate with patients and study sites?

Focus on your interpersonal skills when answering this question. Share how you establish rapport with patients, explain complex information in an understandable manner, and maintain regular contact with study sites through various communication channels to ensure everyone is updated.

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How would you handle a situation where a patient misses their appointment?

Discuss your approach to patient management, emphasizing empathy and understanding. Mention the steps you would take to reschedule the appointment while ensuring the patient feels supported. Talk about the importance of keeping accurate records of such incidents for follow-up.

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Why is attention to detail important in the Clinical Research Coordinator role?

Explain that attention to detail is crucial in clinical research to ensure that all data collected is accurate and compliant with regulatory standards. Give examples of how small errors can have significant consequences and how you ensure precision in your work.

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What software tools are you familiar with that are relevant to this position?

Mention your proficiency with Microsoft Office applications and describe any additional software you’ve used for data management, reporting, or patient communication. Highlight your capacity to quickly learn new technologies as needed in the role.

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How do you ensure the confidentiality and security of patient data?

Discuss the importance of HIPAA compliance and how you implement measures to protect patient information. Explain the protocols you follow to safeguard sensitive data and the ethical considerations you uphold while processing it.

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Can you provide an example of a challenge you faced in a clinical research context and how you resolved it?

Share a specific challenge, such as an unexpected issue during patient recruitment or a data entry mistake. Focus on how you identified the problem, collaborated with your team, and ultimately found a solution that benefited the study.

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What motivates you to work in clinical research?

When answering this, showcase your passion for improving patient care through research. Explain how being part of a team that contributes to advancements in medical aesthetics motivates you, and share times when you felt fulfilled in your role.

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How do you stay updated with changes in clinical research regulations?

Discuss your approach to continuous learning, such as attending workshops, reading relevant literature, or participating in professional organizations. Emphasize your commitment to staying informed to ensure compliance in your work.

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At Cutera, we believe in shaping the future of global aesthetics through the uncompromising pursuit of innovation. We empower our employees to challenge the status quo and create an environment for them to flourish. At Cutera, we embrace a cultu...

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DATE POSTED
March 24, 2025

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