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N-Power Medicine, Inc. · 1 day ago

Clinical Research Coordinator/DHS II - Kansas City 1.14.26

Kansas City, KS

Full-time

Onsite

Mid Level

$99K/yr - $149K/yr

3+ years exp

N-Power Medicine is focused on transforming clinical trials and improving drug development by integrating clinical practice with research. The Clinical Research Coordinator will work directly with healthcare providers and patients to support clinical trials and ensure adherence to study protocols, while also fostering collaborative relationships within the clinical site.

BiotechnologyClinical TrialsPharmaceutical

No H1B

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

Qualification

Oncology clinical researchClinical trial knowledgeCertified Clinical Research CoordinatorPatient consent formsAttention to detailOrganizational skillsCommunication skillsCritical thinkingProblem-solving skills

Required

3+ years of experience in oncology clinical research and/or oncology ambulatory care

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

Preferred

Bachelor's degree, focused in health science or related field

Certified Clinical Research Coordinator, Associate or Professional (CCRC, CCRA or CCRP)

Benefits

Equity at hire

Discretionary annual bonus

Company benefits

Competitive industry benefits

401K plan

Other great company perks

Company

N-Power Medicine, Inc.

N-Power Medicine is developing a radically faster, smarter paradigm for drug development that enables biopharma to move beyond traditional randomized clinical trials.

Founded in 2021

Redwood City, California, USA

51-200 employees