Clinical Research Coordinator/DHS II - Albuquerque, NM 7.21.2026

N-Power Medicine aims to establish a new paradigm in drug development by reinventing the ‘how’ and transforming clinical trials through better integration with clinical practice, ensuring broader participation by physicians and patients. We are building an exceptional multi-disciplinary team with diverse expertise spanning healthcare, engineering, technology and regulatory, and with people who share our core value of Empowering Community through generosity, curiosity and humility. We are working with urgency to bring better therapies to patients faster.

Serve as the Company’s trusted face to the clinical practice, providing clinical support while advancing research data collection.

Interface directly with the healthcare providers and patients.

Perform peer review of clinical documentation for data quality and completeness.

Partner with Senior DHS to address any clinic or team issues and concerns.

Obtain informed consent for N-Power Medicine’s clinical trials.

Assist and participate in the site clinical trial initiation and clinical trial(s) activities as assigned.

Ensure adherence to study protocols, data completeness and patient consent.

Assist in patient recruitment strategies where appropriate.

Foster collaborative relationships by effectively communicating with clinical site staff, internal stakeholders, and the N-Power Medicine team by attending site specific meetings.

Build and maintain relationships at the clinical site, becoming part of the functional team of practitioners.

Ensure quality and integrity of data capture, compliance and confidentiality with N-Power Medicine’s and site’s policies, standard operating procedures (SOPs), and Good Clinical Practice (GCP).

Respond to queries regarding missing, aberrant, or potential outlier data and data verification- escalate to the health care provider as necessary for resolution.

Provide proactive input and user experiences for our software.

Additional duties and responsibilities as required.

Generous, curious and humble.

3+ years of experience in oncology clinical research and/or oncology ambulatory care preferred

Bachelor’s degree, focused in health science or related field preferred

Certified Clinical Research Coordinator, Associate or Professional (CCRC, CCRA or CCRP) preferred

Knowledge of clinical trials, study-specific operating procedures and patient consent forms

Strong desire to drive a paradigm change in clinical research conduct and improve patients’ lives

Compassionate focused patient care

Supports and encourages other team members, contributing to a positive team environment

Self-starter, able to work independently, prioritize actively, seek input, and problem solve in complex and fast-evolving environments

Results oriented focused on delivering the goals set-forth

Attention to detail and strong organizational skills

Excellent oral/written communication and interpersonal skills

Critical thinking and proven problem-solving skills

Work hours are dependent on local Network Partner Clinics (typically M-F, 8-5pm)

Daily travel between sites may be required