Sr. Clinical Research Associate; Cardiac Catheter Products

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  to learn more.

• 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.

• 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.

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).

• 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…