Clinical Research Associate

Embark on an enriching journey with PROCEPT Bio Robotics, where our vision, mission, and values guide everything we do as a company. At PROCEPT, we put the patient first in everything we do and are committed to revolutionizing treatment for benign prostatic hyperplasia (BPH, otherwise known as prostate gland enlargement) through innovation in surgical robotics. As our company succeeds and grows, we improve the quality of life of patients, provide more effective treatment options for surgeons, uphold the trust of our shareholders.

That starts with a commitment to our People with a focus on creating an evolving landscape for your career, brimming with transformative opportunities that provide continuous career growth opportunities.

Are you ready to embark on an exciting journey that will revolutionize the way men suffering from BPH and prostate cancer are treated? Join us as a Clinical Research Associate, where you will play a key role in supporting clinical trials from start to finish. You will assist in developing protocols, case report forms, and consent documents while ensuring compliance with good clinical practices.

Your responsibilities will also include site selection, investigator engagement, and study monitoring. This role offers opportunities for growth, including exposure to Regulatory Affairs.

Embark on an enriching journey with PROCEPT Bio Robotics, where our vision, mission, and values guide everything we do as a company. At PROCEPT, we put the patient first in everything we do and are committed to revolutionizing treatment for benign prostatic hyperplasia (BPH, otherwise known as prostate gland enlargement) through innovation in surgical robotics. As our company succeeds and grows, we improve the quality of life of patients, provide more effective treatment options for surgeons, uphold the trust of our shareholders.

That starts with a commitment to our People with a focus on creating an evolving landscape for your career, brimming with transformative opportunities that provide continuous career growth opportunities.

• Ensure that documentation from investigators and investigational sites meets FDA/GCP/ICH requirements
• Assist in implementing clinical research projects
• Review case report forms and informed consent forms against the study protocol and other governing documents to allow for accurate and thorough data collection to support the product through the regulatory approval process
• Assist site coordinators, investigators, field clinical staff, CRO (as applicable) in collecting data in a timely manner that meets the protocol requirements
• Organize data in systematic manner to allow for efficient and accurate clinical reports
• Perform joint site visits with other CRAs to ensure regulatory and study requirements are being fulfilled

• Bachelor's degree in a scientific or health care discipline preferred and/or training; or equivalent combination of education and experience
• 2+ years' recent experience in clinical role
• Excellent verbal and written communication skills
• Excellent organizational skills along with strong attention to detail
• Ability to work both independently and collaboratively with cross-functional teams
• Highly proficient with Microsoft Office Suite
• Ability to travel approximately 35-40%

At PROCEPT, we believe every person matters. Every employee, every patient, every caregiver. Because we are here to create a revolution, and we believe in doing that by innovating everywhere with pathological optimism. We believe in being humble and highly engaged in the work we do, while also working together seamlessly for a common goal. At Procept, curiosity, ingenuity and conviction in the power technology will transform the lives of our patients and providers.

And this doesn’t happen by accident. It starts with our live induction program that serves as an incubator for cross-functional team building, an immersion in Procept’s history, jam-packed interactive sessions with executive leadership and a crash-course in the mission and purpose of what we do. It…