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N-Power Medicine

Accelerates cancer therapy development for pharma

Digital Health Specialist 2

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeTraverse City, MI, USA$99k - $149k /yr

About the Job

Requirements

  • Three or more years of experience in oncology clinical research and/or oncology ambulatory care is preferred.
  • A bachelor's degree focused in health science or a related field is preferred.
  • Knowledge of clinical trials, study-specific operating procedures, and patient consent forms.
  • Ability to provide compassionate, focused patient care.
  • Ability to work independently, prioritize tasks, seek input, and solve problems in complex, fast-evolving environments.
  • Attention to detail and strong organizational skills.
  • Critical-thinking and problem-solving skills.
  • Excellent oral and written communication and interpersonal skills.
  • Work hours depend on local network partner clinics, typically Monday through Friday, 8 a.m. to 5 p.m.
  • Applicants must be currently authorized to work in the United States on a full-time basis.

Responsibilities

  • Provide clinical support to the clinical practice while advancing research data collection.
  • Interface directly with healthcare providers and patients.
  • Peer-review clinical documentation for data quality and completeness.
  • Partner with Senior Digital Health Specialists to address clinic or team issues and concerns.
  • Obtain informed consent for the company's clinical trials.
  • Assist with and participate in site clinical trial initiation and trial activities as assigned.
  • Ensure adherence to study protocols, data completeness, and patient consent.
  • Assist with patient recruitment strategies where appropriate.
  • Attend site-specific meetings and communicate with clinical site staff, internal stakeholders, and the company team to foster collaborative relationships.
  • Build and maintain relationships at the clinical site and become part of the functional team of practitioners.
  • Ensure the quality and integrity of data capture, compliance, and confidentiality in accordance with company and site policies, standard operating procedures, and Good Clinical Practice.
  • Respond to queries about missing, aberrant, or potential outlier data and data verification, escalating to the healthcare provider as necessary for resolution.
  • Provide proactive input and user feedback for the company's software.
  • Travel daily between clinical sites.

Desired Qualifications

  • Certification as a Clinical Research Coordinator, Associate, or Professional (CCRC, CCRA, or CCRP) is preferred.

About the Company

N-Power Medicine

Accelerates cancer therapy development for pharma

N-Power Medicine focuses on oncology-related drug development services. It accelerates the creation of cancer therapies by partnering with pharmaceutical companies and research institutions, leveraging advanced technologies and innovative methods to shorten development timelines and bring effective treatments to patients faster. The company’s services are delivered through collaborations, earning revenue from service fees, research grants, and potential licensing of its proprietary technologies. Compared with competitors, it emphasizes specialized oncology expertise, active partnerships, and a workflow that combines research services with opportunities for licensing, aiming to streamline development rather than just offer generic research support. The goal is to improve patient outcomes by speeding up the availability of effective cancer treatments.

Company size
51-200
Company stage
Series B
Total funding
$32M
Headquarters
Redwood City, CA
Founded
2021

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