Clinical Research Coordinator
Behavioral Health Market Context
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Benefits
The expected salary range for this position is $99,000 and $149,000Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by lawN-Power Medicine (NPM) offers equity at hire as well as a discretionary annual bonus which may be available based on Company performanceThis position is eligible for company benefits1 more items(s)
Qualifications
- •The ideal candidate has clinical oncology research experience
- •You are confident in your understanding of clinical workflow, patient data systems and clinical research in an oncology setting
- •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)
- •Generous, curious and humble
- •Applicants must be currently authorized to work in the U.S. on a full-time basis
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Responsibilities
- •You will be a part of the rapidly changing clinical oncology environment with the opportunity to impact the future of clinical research and improve patients’ lives while growing professionally at a dynamic, fast-growing, start-up organization
- •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
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