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ProvidencePosted 27 days ago

Clinical Research Coordinator - Per diem

Full-time
On-site
2+ years
Competitive
Posted 27 days ago

Providence is hiring a Clinical Research Coordinator to oversee the day-to-day functions of multiple clinical research studies. The role coordinates with the Principal Investigator, patients, sponsors, and the IRB, and ensures accurate, timely documentation and compliance with study protocols.

Posted
27 days ago
Source
providence.jobs
Sector
Healthcare

Opens the employer's application page in a new tab

Responsibilities

  • Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies
  • This role is responsible for interfacing with the Principal Investigator, Patient, Sponsor, and the IRB
  • This position is directly responsible to ensure that all documentation is timely and accurate and works closely with the PI to ensure strict compliance to study protocols (GCP/ICH)

Qualifications

  • Completion of an accredited Medical or Phlebotomy training program, or equivalent educ/experience

Preferred

  • Graduate of a Vocational School or college
  • Coursework/Training: Biohazardous Material packaging training
  • F02 AMG Clinical Trials: Required to have College Degree
  • Upon hire: Phlebotomy Certificate (for department SJuHMG Clinical Trials)
  • 2 years experience in a Clinical Research setting
  • 3 years preferred
  • College Degree
  • Biohazardous Material Packaging Training
  • 2+ Years Clinical Research Experience
  • 3+ Years Clinical Research Experience (Preferred)

Required skills

Biohazardous Material PackagingPhlebotomy

Full job description

Providence is hiring a Clinical Research Coordinator to oversee the day-to-day functions of multiple clinical research studies. The role coordinates with the Principal Investigator, patients, sponsors, and the IRB, and ensures accurate, timely documentation and compliance with study protocols.

Responsibilities

  • Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies
  • This role is responsible for interfacing with the Principal Investigator, Patient, Sponsor, and the IRB
  • This position is directly responsible to ensure that all documentation is timely and accurate and works closely with the PI to ensure strict compliance to study protocols (GCP/ICH)

Preferred

  • Graduate of a Vocational School or college
  • Coursework/Training: Biohazardous Material packaging training
  • F02 AMG Clinical Trials: Required to have College Degree
  • Upon hire: Phlebotomy Certificate (for department SJuHMG Clinical Trials)
  • 2 years experience in a Clinical Research setting
  • 3 years preferred
  • 2 years experience in a Clinical Research setting.
  • 3 years preferred.
  • Vocational School Graduate
  • College Degree
  • Biohazardous Material Packaging Training
  • Phlebotomy Certificate
  • 2+ Years Clinical Research Experience
  • 3+ Years Clinical Research Experience (Preferred)

Benefits

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

Company

  • Not-for-profit faith-based hospital and clinic health care system
  • Renton, Washington, USA
  • https://www.providence.org/
  • Founded in 1859
  • 10001+ employees

Qualifications

  • Completion of an accredited Medical or Phlebotomy training program, or equivalent educ/experience
  • Graduate of a Vocational School or college
  • Coursework/Training: Biohazardous Material packaging training
  • F02 AMG Clinical Trials: Required to have College Degree
  • Upon hire: Phlebotomy Certificate (for department SJuHMG Clinical Trials)
  • 2 years experience in a Clinical Research setting
  • 3 years preferred

Required skills

  • Biohazardous Material Packaging, Phlebotomy

Preferred skills

  • 2 years experience in a Clinical Research setting, 3 years preferred, F02 AMG Clinical Trials: Required to have College Degree, Graduate of a Vocational School or college

Experience

  • 2+ years

Job details

Employment type

Full-time

Seniority level

2+ years

Date posted

Oct 17, 2026

Work mode

On-site

Job source

providence.jobs

Company

Providence

Healthcare

Not-for-profit faith-based hospital and clinic health care system

See all 4 jobs from Providence →
  • Renton, Washington, USA
  • Healthcare
  • 10001+ employees
  • Founded 1859
  • providence.org

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