Clinical Research Coordinator/DHS II - Traverse City, MI 10.28.2026
About The Position
N-Power Medicine is seeking a Clinical Research Coordinator, internally titled Digital Health Specialist II, to work across multiple clinical sites in the Traverse City area. The role provides clinical support to oncology practices while advancing clinical research data collection, with the opportunity to contribute to clinical trials and improve patient care in a fast-growing startup environment. The coordinator works directly with healthcare providers and patients, supports clinical trial initiation and activities, obtains informed consent, and helps ensure adherence to study protocols and the completeness and integrity of research data. The role also involves reviewing clinical documentation, responding to data queries, supporting patient recruitment, communicating with site staff and internal teams, and providing feedback on the company’s software. Daily travel between sites is required. 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; the company will not sponsor work visas. Employment is contingent on successfully passing applicable background checks and screenings. The position offers equity at hire, a discretionary annual bonus that may be available based on company performance, and company benefits.
Requirements
- Knowledge of clinical trials, study-specific operating procedures, and patient consent forms.
- Compassionate, patient-focused care.
- Ability to support and encourage team members and contribute to a positive team environment.
- Ability to work independently, prioritize, seek input, and solve problems in complex, fast-evolving environments.
- Results-oriented approach focused on delivering goals.
- Attention to detail and strong organizational skills.
- Excellent oral and written communication and interpersonal skills.
- Critical thinking and proven problem-solving skills.
- Currently authorized to work in the United States on a full-time basis; visa sponsorship is not available.
- Successful completion of applicable background checks and screenings.
- Availability for work hours determined by local Network Partner Clinics, typically Monday through Friday, 8 a.m. to 5 p.m., and daily travel between sites.
Nice To Haves
- Three or more years of experience in oncology clinical research and/or oncology ambulatory care.
- Bachelor’s degree focused in health science or a related field.
- Certified Clinical Research Coordinator, Associate, or Professional (CCRC, CCRA, or CCRP).
- Clinical oncology research experience or research experience in a healthcare setting.
- Confident understanding of clinical workflow, patient data systems, and clinical research in an oncology setting.
- Strong desire to drive change in clinical research and improve patients’ lives.
- Generosity, curiosity, and humility.
Responsibilities
- Serve as the company’s trusted representative to clinical practices, providing clinical support while advancing research data collection.
- Interface directly with healthcare providers and patients.
- Peer-review clinical documentation for data quality and completeness.
- Partner with a Senior Digital Health Specialist to address clinic or team issues and concerns.
- Obtain informed consent for N-Power Medicine clinical trials.
- Assist with and participate in site clinical trial initiation and assigned trial activities.
- Ensure adherence to study protocols, data completeness, and patient consent.
- Assist with patient recruitment strategies where appropriate.
- Communicate with clinical site staff, internal stakeholders, and the N-Power Medicine team, including attending site-specific meetings.
- Build and maintain relationships at clinical sites and become part of the functional team of practitioners.
- Ensure 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 regarding missing, aberrant, or potential outlier data and data verification, escalating to healthcare providers as necessary.
- Provide proactive software input and user experience feedback.
- Perform additional duties and responsibilities as required.
- Travel daily between clinical sites.
Benefits
- Equity at hire.
- A discretionary annual bonus may be available based on company performance.
- Company benefits.
- Competitive industry benefits.
- 401(k) plan.
- Balanced and flexible work environment.
- Other company perks.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
