Associate Clinical Research Analyst - Tumor Research Institute

Providence

Seattle (WA)

On-site

USD 70,000 - 95,000

Full time

2 days ago
Be an early applicant

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Job summary

You will manage IRB submissions to protect human subjects, assist with FDA filings as needed, and lead Research Assistants on task-based work while setting priorities and timelines to support project objectives.

Qualifications

  • Bachelor's Degree preferably in science, healthcare, pharmacy, or other related field., Or Significant experience in research coordination or regulatory work may be substituted for educational requirements.
  • 2 years experience in healthcare, research or clinical setting with regulatory compliance familiarity.

Responsibilities

  • Prepares, facilitates, coordinates, and submits documentation required by federal, state and local regulations and institutional requirements relating to the conduct of research.
  • Leads the work of Research Assistants on a task-basis if applicable. Provides on-the-job training, sets priorities and schedules workflow required to support project objectives.

Skills

Regulatory compliance
IRB submissions

Education

Bachelor's Degree in science, healthcare, pharmacy, or related field

Job description

Prepares, facilitates, coordinates, and submits documentation required by federal, state and local regulations and institutional requirements relating to the conduct of research. This includes preparation of all submissions to the IRB to assure the protection of human subjects in research; FDA-required submissions which may include investigator 1572 forms, investigational new drug applications, device submissions such as Emergency use, HDE, Safety Reports, and other documents that may be required by a regulatory agency or the institution. Leads the work of Research Assistants on a task-basis if applicable. Provides on-the-job training, sets priorities and schedules workflow required to support project objectives.

Providence caregivers are not simply valued – they’re invaluable. Join our team atSwedish Researchand thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them.

Required Qualifications:
  • Bachelor's Degree preferably in science, healthcare, pharmacy, or other related field., Or Significant experience in research coordination or regulatory work may be substituted for educational requirements.
  • 2 yearsexperience in healthcare, research or clinical setting with regulatory compliance familiarity.
Why Join Providence?

Ourbest-in-class benefitsare uniquely designed to support you and your family in staying well, growing professionally, and achieving financial security. We take care of you, so you can focus on delivering ourMissionof caring for everyone, especially the most vulnerable in our communities.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Associate Clinical Research Analyst - Tumor Research Institute
Associate Clinical Research Analyst - Tumor Research Institute

Swedish • Seattle (WA)

Hybrid
USD 43,000 - 66,000
Clinical Research Regulatory Coordinator
Clinical Research Regulatory Coordinator

Swedish • Seattle (WA)

Hybrid
USD 43,000 - 66,000
Associate Clinical Research Analyst - Tumor Research Institute
Associate Clinical Research Analyst - Tumor Research Institute

Swedish • Seattle (WA)

Hybrid
USD 43,000 - 66,000
401(k) match
Health insurance
Life insurance
+4
Clinical Regulatory Submissions Specialist
Clinical Regulatory Submissions Specialist

Providence Swedish Medical Center • Seattle (WA)

Hybrid
USD 43,000 - 66,000
401(k) match
Health insurance
Life insurance
+4
Clinical Research Regulatory Analyst — IRB & FDA Submissions
Clinical Research Regulatory Analyst — IRB & FDA Submissions

Providence • Seattle (WA)

On-site
USD 70,000 - 95,000
Clinical Research Coord
Clinical Research Coord

University of Utah • Salt Lake City (UT)

On-site
USD 65,000 - 90,000
Clinical Research Budgeting Analyst - Clinical Trials
Clinical Research Budgeting Analyst - Clinical Trials

Providence Swedish Medical Center • Portland (OR)

Remote
USD 85,000 - 120,000
Specialist - Research Quality and Assurance
Specialist - Research Quality and Assurance

Memorial Healthcare System • Florida

On-site
USD 70,000 - 110,000
Clinical Research Coordinator - Trials & Compliance Leader
Clinical Research Coordinator - Trials & Compliance Leader

Providence • Mission Viejo (CA)

On-site
USD 46,000 - 71,000
Research Regulatory Assistant
Research Regulatory Assistant

Brown University Health • Providence (RI)

On-site
USD 42,000 - 69,000