Clinical Research Coordinator

Benefits

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
• •12 more items(s)