Clinical Research Coordinator

Posted 2 Days Ago
Be an Early Applicant
Honolulu, HI, USA
In-Office
Mid level
Healthcare Services
The Role
Coordinates early-phase oncology clinical trials, including protocol activation, patient identification and enrollment, informed consent, patient follow-up, data collection, regulatory compliance, quality control, and collaboration with investigators, nurses, physicians, and clinical operations staff. Maintains accurate clinical and research records while following ICH Good Clinical Practice, human-subjects research standards, and HIPAA requirements.
Summary Generated by Built In

APPLICANTS MUST RESIDE IN HAWAII

Duties & Responsibilities:

  • Independently organizes and manages activities and tasks associated with the conduct of early-phase industry-sponsored and investigator-initiated cancer clinical trials in the Ho‘ōla Early-Phase Clinical Research Center (EPCRC). 
  • Works with the clinical trial operation team to identify and inform candidate patients about available clinical protocols, enrolls consenting eligible patients and follows enrolled patients. 
  • Collects, documents, and enters data accurately and timely into case report forms, electronic medical record, and electronic data capture systems as required per protocol.
  • Works with the clinical operation staff to ensure standard of care procedures are identified. Responsible for multiple functions needed to access, select and activate protocols and to maintain a high level of training, continuing education, quality control, and regulatory compliance for the enterprise. 
  • Works closely with the PI and his/her designee, with nurses and other staff in EPCRC, and with physicians/investigators to foster strong working relationships to ensure compliance with the conduct of industry and investigator-initiated research. 
  • Follows the standards and practices of the International Conference on Harmonization for Good Clinical Practices.  
  • Handles confidential information responsibly. Maintains confidentiality of patient information in accordance with Health Insurance Portability and Accountability Act (HIPAA). 
  • Maintains training as required in human subjects’ research and all other requirements of UHP.      
  • Complies with all legal requirements and company policies.
  • Performs all other duties as assigned.     

Please see the attached job description for more information.

QUALIFICATION REQUIREMENTS

Education/Training/Experience

Minimum:

  • Bachelor’s Degree from an accredited four (4) year college or university in a health-related field, or an equivalent number of years of relevant healthcare experience. Relevant education, training, and professional experience in a health-related field may be considered in place of a degree.
  • Three (3) years of experience working in health research/clinical trials including at least one year of oncology OR 5 years working in a health care clinic setting.

Preferred:

  • Advanced Degree from an accredited college or university in a related field.
  • Previous experience of early-phase industry-sponsored and investigator-initiated cancer clinical trials is preferred.

 

Skills Knowledge

Minimum: 

  • Works autonomously with minimal supervision, while also understanding the boundaries of the role, responsibilities, and experience. Seeks guidance and clarification from appropriate protocol-involved personnel when necessary.
  • Demonstrated knowledge in human subjects’ research and International Conference on Harmonization (ICH) 
  • Demonstrated knowledge in Good Clinical Practices (GCP) 
  • Demonstrated knowledge in Health Insurance Portability and Accountability Act (HIPAA) requirements     . 
  • Understanding of research study designs and ethics. 
  • Knowledge of and experience with computers and software programs, including word-processing, spreadsheets, and databases. 
  • Specialized knowledge of specific cancer care sites conducting clinical trials or of job areas, such as education/training, regulatory, investigational drug accountability/storage, specimen collection/processing, database maintenance/reporting, and regulatory compliance auditing.      
  • Demonstrates strong organizational skills, attention to detail, accuracy, desire to learn, and timeliness of work. 
  • Strong and effective written and verbal communication skills, and interacts with supervisors, co-workers, and others respectfully and professionally at all times.

 

BENEFITS

  • Generous time off benefits
  • 100% employee health and dental coverage and vision
  • Flexible spending plan  
  • Identity & fraud protection
  • Supplemental insurance (Accident, Critical Illness and Hospital benefit)  
  • 100% company paid group Life/AD&D/LTD insurance  
  • Retirement plan with up to 3% dollar-for-dollar company matching contributions
  • Employee assistance program (EAP)
  • Pet Insurance, Prepaid legal with competitive rates


 

UHP Hawai‘i is an EEO/AAP employer.

Skills Required

  • Bachelor’s degree from an accredited four-year college or university in a health-related field, or equivalent relevant healthcare experience
  • Three years of experience working in health research or clinical trials, including at least one year of oncology experience
  • Alternatively, five years of experience working in a healthcare clinic setting
  • Knowledge of human subjects research and International Conference on Harmonisation (ICH) standards
  • Knowledge of Good Clinical Practice (GCP)
  • Knowledge of HIPAA requirements
  • Understanding of research study designs and ethics
  • Experience with computers and software programs, including word processing, spreadsheets, and databases
  • Specialized knowledge of cancer care sites conducting clinical trials or related areas such as regulatory operations, investigational drug accountability, specimen processing, database reporting, or compliance auditing
  • Advanced degree in a related field
  • Previous early-phase industry-sponsored and investigator-initiated cancer clinical trial experience
  • Residence in Hawaii
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The Company
HQ: Honolulu, Hawaii
105 Employees
Year Founded: 2005

What We Do

University Health Partners of Hawaii provides high-quality healthcare through outpatient clinics and public school based health services, through the Hawaii Keiki: Healthy and Ready to Learn program. We are dedicated to supporting the clinical, educational, research, and community service activities of the University of Hawaii Health Sciences Programs.

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