Oncology Clinical Trials Coordinator

Npowermedicine; Philadelphia (Philadelphia County); On-site; USD 70,000 - 95,000; Full time

Benefits offered by this job

401K plan

Flexible work environment

Competitive compensation

Job summary

N-Power Medicine is seeking a Digital Health Specialist II to join a fast-growing oncology-focused clinical research team at a clinical site in Philadelphia, PA. You will support data collection, consent processes, and coordination with healthcare providers to advance trials and improve patient care.

The ideal candidate has oncology research experience in a healthcare setting, strong data management and communication skills, and a proactive, independent work style to thrive in a dynamic startup

Qualifications

• 3+ years of experience in oncology clinical research or oncology ambulatory care.
• Bachelor’s degree 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, patient-focused care.
• Self-starter, able to work independently, prioritize actively, seek input, and problem solve in complex environments.
• Attention to detail and strong organizational skills.
• Excellent oral and written communication and interpersonal skills.
• Typical work hours are Monday–Friday, 8–5 depending on site schedules.

Responsibilities

• 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 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 site staff, internal stakeholders, and the N-Power Medicine team.
• 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 SOPs and GCP.
• Respond to queries regarding missing, aberrant, or potential outlier data and escalate as necessary.
• Provide proactive input and user experiences for our software.
• Additional duties as required.

Skills

Oncology clinical research experience

Clinical data collection

Communication skills

Attention to detail

Problem solving

Organizational skills

Team collaboration

Education

Bachelor's degree in health science or related field

CCRC/CCRA/CCRP certification preferred

Job description

N-Power Medicine is seeking a Digital Health Specialist II to join a fast-growing oncology-focused clinical research team at a clinical site in Philadelphia, PA. You will support data collection, consent processes, and coordination with healthcare providers to advance trials and improve patient care.

The ideal candidate has oncology research experience in a healthcare setting, strong data management and communication skills, and a proactive, independent work style to thrive in a dynamic startup