Clinical Research Coordinator 2

Salary Range: 99000 to 149000 (Currency: USD) (Pay period: per-year-salary)

Roles and 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(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. 
• Generous, curious and humble.

Qualifications

• 3+ years of experience in oncology clinical research and/or oncology ambulatory care preferred
• Bachelor’s degree, focused 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 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)
 
 
Please note that state-specific background checks and screenings may be required for this role. Employment is contingent upon successfully passing all applicable screenings.

Travel Requirements

• Daily travel between sites may be required