Sr. Clinical Research Associate (Cardiac Catheter Products) at Pulse Biosciences

United States

Pulse Biosciences (Nasdaq: PLSE): Join the Future of Bioelectric Medicine Pulse Biosciences is a novel bioelectric medicine company committed to health innovation that has the potential to improve the quality of life for patients. The Company’s proprietary CellFX® nsPFA™ (nanosecond Pulsed Field Ablation) technology delivers nanosecond pulses of electrical energy to non-thermally ablate cells while sparing adjacent noncellular tissue. The Company is actively pursuing the development of its CellFX nsPFA technology for use in the surgical treatment of atrial fibrillation and percutaneously in a select few other markets where it could have a profound positive impact on healthcare for both patients and providers. Visit pulsebiosciences.com to learn more. Why Join Us? At Pulse Biosciences, we are driven by purpose and innovation. Our Mission: To build a viable Company that designs, produces, and commercializes nano-pulse technology to improve and extend the lives of patients. To solve the needs of patients, physicians, and healthcare providers with high quality and high reliability products and services, developed in accordance with rigorous scientific, engineering, and clinical standards. We exist to make a positive difference in the lives of patients, physicians, healthcare providers, shareholders and our Pulse Biosciences team members. Our Culture: A community of creative, forward-thinking individuals tackling challenges with ingenuity and collaboration. Our Commitment: Hiring the best and brightest minds to advance our world-class organization. What You Will Experience: Culture and Purpose - Purposeful and rewarding work collaborating with bright and curious minds brings us together! Innovative Environment - An environment that fosters innovation to take products from concept to human use quickly! Growth Opportunities - Learning culture focusing on professional and personal growth and development that you can only get in a startup-like environment! Comprehensive Benefits - A variety of health insurance plans and supplemental insurance options, and 401k retirement savings plan. Ownership and Rewards - Stock options awards and Employee Stock Purchase Plan (ESPP) to share in our success. Work-Life Balance - Enjoy paid time off, paid holidays, flexible work schedule and wellness program, including onsite gym and mindfulness classes. Diversity & Inclusion - A commitment to providing a respectful work environment to our diverse workforce. About the Role As the Sr. Clinical Research Associate (Sr. CRA) you’ll be responsible for managing and monitoring activities that will lead to successful execution of clinical studies at US and international clinical sites. You will monitor patient recruitment, data and study related information related to clinical sites and study participation. Ensure that duties are performed in accordance with the Code of Federal Regulations (CFR) of the Food and Drug Administration (FDA) and the International Conference on Harmonization - Good Clinical Practice (ICH-GCP). To Make an Impact, You Will: Provide case support to research sites across multiple studies with minimal guidance. Prepare and develop project and study-related documents including informed consent forms, CRFs, study guides, study reference binders, and patient diaries. Coordinate review of data listings and preparation of interim and final clinical study reports. Be responsible for monitoring clinical studies, which includes review of case report forms (CRFs) both paper and/or electronic data capture (EDC), and source documentation to ensure adherence to the protocol and scientific validity of the data. Be responsible for developing study specific monitoring tools and other related documents. Deliver high quality written monitoring reports, confirmation and follow-up letters within the timelines of SOPs and monitoring plans. Ensure that all missing action items (MAIs) from monitoring visits are closed within the timelines of monitoring plans. Be responsible for reviewing and approving essential regulatory documents across multiple studies. Assist the project team in developing study metrics to ensure the efficient execution of a clinical trial. Oversee clinical data to ensure queries are closed within stipulated timelines of study goals Provide clinical support for submission of trials to IRB/IEC and regulatory authorities. Ensure adherence to study timeline across multiple studies. Coach and mentor other Clinical Research Associates (CRAs) in development and training. Maintain strong working knowledge of protocols and product development across multiple studies. Demonstrate ability to coordinate, organize, communicate, and manage site activities, with knowledge of when to escalate issues to management or clinical team. Demonstrate an excellent working knowledge of clinical research processes, Good Clinical Practices, International Committee on Harmonization Guidelines, federal regulations and applicable local laws pertaining to clinical research investigations. Verify the rights and well-being of study subjects are protected and verifies that written informed consent was obtained before each subject’s participation in the study. Perform Investigational Product accountability, including product storage, inventory, return/destruction, and dispensing/receipt records. Ensure compliance in reporting adverse events/serious adverse events according to the protocol and applicable regulatory agencies. Manage Protocol Deviation documentation, tracking, and escalation. Participate in site audits, as requested. To Excel, You Will Bring: BS/BA degree or equivalent experience. 5+ years’ experience directly supporting clinical research or relevant experience in medical/scientific area. At least 3 years of CRA experience in device or biotech clinical trials. Cardiovascular device experience preferred Certified as a CRA, e.g. CCRA, CCRP, or other CRA certification strongly preferred. Proficient in Acrobat Adobe, Microsoft Word, Excel, Power Point, and Smartsheet; and the ability to quickly become proficient in a variety of other computer software programs. Knowledge of FDA and international regulations and guidelines including, but not limited to, clinical strategy, GCPs, SOPs, submissions, product launch, labeling, advertising and promotion, product vigilance and medical device reporting. Proficient in using EDC and CTMS systems. Working knowledge of FDA, European Regulatory and EC procedures, as applicable. Excellent oral, written communication skills with strong presentation skills. Clear and systematic thinking that demonstrates good judgment and problem-solving competencies. Excellent critical thinking analytical skills. Strong organizational skills with the ability to work conscientiously and with minimal direction, using good judgment, taking initiative to accomplish short and long-range projects, and recommend actions with minimal direction. Ability to work as a team member, multi-task and be very flexible to adapt to the ever-changing work priorities and requirements of a dynamic, fast growing company. Flexibility in work hours and readiness to travel 30%-50% of the time, overnight and/or international travel may be required. Ability to lift 10-15 pounds. Ready to Shape the Future of Healthcare? Apply today to join Pulse Biosciences and help us redefine the boundaries of medicine with bioelectric innovation. To learn more about us, visit our website at www.pulsebiosciences.com. We provide equal employment opportunities (EEO) to all persons regardless of race, age, color, gender, sexual orientation, national origin, physical or mental disability, religion, or any other characteristic protected by federal, state or local law. We will make reasonable accommodations for qualified individuals with disabilities. PRINCIPALS ONLY; UNSOLICITED CANDIDATE SUBMISSIONS FROM RECRUITERS OR THIRD-PARTY AGENCIES WILL BE CONSIDERED FREE REFERRALS.