Associate Clinical Research Coordinator - Cancer Research

Providence Health & Services is hiring an Associate Clinical Research Coordinator to coordinate and maintain clinical trials at the John Wayne Cancer Institute. The role supports patient screening and follow-up, study data quality and submission, and collaboration with investigators, sponsors, and clinical research nurses.

Responsibilities

• The Clinical Research Associate I will function under the supervision of the Clinical Research Supervisor, coordinating and maintaining diverse activities related to clinical trials at the John Wayne Cancer Institute
• This includes, but is not limited to: patient screening, eligibility, registration, quality control of data compilation and submission, study evaluation, as well as direct patient follow-up by phone
• Interacts closely with institutional investigators and industry sponsors
• Collaborates with the Clinical Research Nurses throughout study completion
• Must uphold the standards of confidentiality, attendance and punctuality
• Performs all duties in a manner, which promotes team concept and reflects the Sisters of Providence mission and philosophy

Preferred

• Upon hire: ACRP or SOCRA certification, or other Clinical Research Certification
• 1 year experience with Phase I-II trials
• Oncology experience
• Experience with Electronic Data Capture systems (InForm, Medidata Rave, etc.)
• 1 year experience with Phase I-II trials.
• ACRP Certification
• SOCRA Certification
• Clinical Research Certification
• Phase I–II Trial Experience
• Oncology Experience
• Electronic Data Capture (EDC)
• InForm
• Medidata Rave

Benefits

• Additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities.
• Retirement 401(k) Savings Plan with employer matching
• Health care benefits (medical, dental, vision)
• Life insurance
• Disability insurance
• Paid parental leave
• Paid vacations
• Paid holidays
• Paid time off for health issues
• Voluntary benefits
• Well-being resources

Company

• Healthcare provider operating hospitals, clinics, and social services
• Renton, Washington, USA
• https://www.providence.org/
• Founded in 1859
• 10001+ employees

Qualifications

• Bachelor's Degree, r equivalent education/experience
• 1 year of Clinical research coordination, or 2 years of clinical research data entry or equivalent experience in Clinical Trials
• Upon hire: ACRP or SOCRA certification, or other Clinical Research Certification
• 1 year experience with Phase I-II trials
• Oncology experience
• Experience with Electronic Data Capture systems (InForm, Medidata Rave, etc.)
• 1 year of Clinical research coordination, or 2 years of clinical research data entry or equivalent experience in Clinical Trials.

Required skills

• ACRP Certification, Clinical Research Coordination, Clinical Research Data Entry, Clinical Trials, InForm, Medidata Rave, Oncology, Phase I–II Clinical Trials, SOCRA Certification

Preferred skills

• 1 year experience with Phase I-II trials, Oncology experience

Experience

• 1+ years