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.
Requirements
- In depth knowledge of clinical trials, study-specific operating procedures and patient consent forms
Responsibilities
- Serve as the Company’s trusted face to the clinical practice, providing clinical support while advancing research data collection.
- Manage queries regarding missing, aberrant, or potential outlier data for studies and projects - escalate to the healthcare provider and Digital Health staff as necessary for resolution.
- 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.
- Ensure quality and integrity of the Kaleido Registry and clinical trials data, protocol compliance and confidentiality with N-Power Medicine’s and site’s policies, standard operating procedures (SOPs), and Good Clinical Practice (GCP).
- Collect practice insights regarding Kaleido Registry workflows and maintain site performance metrics for internal and site reporting.
- Provide proactive input and user experiences including software- escalate issues while offering solutions based upon your expert knowledge and experience.
Other
- Act as the point of contact for network partners and N-Power Medicine staff supporting the site to address queries and issues in a timely manner.
- Participate directly in the implementation at the site and all aspects of a site start-up.
- Support the hiring and onboarding of new N-Power Medicine staff including, new hire interviews, new hire training, onsite shadowing, etc.
- Perform quality assurance activities as required, identify opportunities for retraining of Digital Health Staff.
- Assist in developing training, work instructions and standard operating procedures, and other materials.
- Obtain informed consent for N-Power Medicine’s clinical trials.
- Lead patient recruitment strategies where appropriate as site liaison and network partner research department.
- Foster collaborative relationships by effectively communicating with clinical site staff, internal stakeholders, and N-Power Medicine.
- Attend, participate and take action in required meetings.
- Build and maintain relationships at the clinical site, becoming part of the functional team of practitioners.
- Solicit feedback from users of new technology and contribute to implementation for clinical care and clinical trials.
- 5+ years of experience in oncology clinical research and/or oncology ambulatory care
- Bachelor’s degree, focused in health science or related field
- Clinical supervisory or management experience preferred
- Certified Clinical Research Coordinator, Associate or Professional (CCRC, CCRA or CCRP) preferred
- Bilingual in Spanish (or other language) is preferred
- Strong desire to drive a paradigm change in clinical research conduct and improve patients’ lives
- Compassionate focused patient care
- Coach 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
- Exceptional oral and written communication skills with a proven ability to lead through effective interpersonal interactions at all organizational levels
- Critical thinking and proven problem-solving skills
- Work hours are dependent on local Network Partner Clinics (typically M-F, 8-5pm)
- Generous, curious and humble.
- Daily travel between network partner sites may be required
- Applicants must be currently authorized to work in the U.S. on a full-time basis.
- The Company will not sponsor applicants for work visas.
- Please note that state-specific background checks and screenings may be required for this role.
- Employment is contingent upon successfully passing all applicable screenings.
