Top 56 regulatory affairs Jobs in bothell wa

Clinical Research Coordinator II - Experienced | Rheumatology Research
Confidential —Bellevue, WA
- $32 - $36 an hour
- Full-time
- Vital signs
- Laboratory experience
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Director of Regulatory Compliance-Oral Healthcare
Philips —Bothell, WA
- $172,200 - $275,520 a year
- Full-time
- 11+ years
- Office
- Bachelor's degree
- Health savings account
- Employee stock purchase plan
Senior Regulatory Affairs Specialist
Philips —Bothell, WA
- $105,000 - $168,000 a year
- Full-time
- 5 years
- Office
- Travel
- Health savings account
- Employee stock purchase plan
Medical Science Liaison, Oncology (Northern CA, OR, WA, MT, ID)
Jazz Pharmaceuticals —Seattle, WA
- $160,000 - $240,000 a year
- Medicine
- RN License
- English
- Health insurance
- Dental insurance
11d
Post Market Surveillance Specialist
Katalyst Healthcares & Life Sciences —Bothell, WA
- Contract
- Bachelor's degree
- Senior level
- 4 years
Quick Apply
8d
Post Market Surveillance (PMS) Specialist
Katalyst Healthcares & Life Sciences —Bothell, WA
- Contract
- Bachelor's degree
- Senior level
- 4 years
Quick Apply
12d
Economic Development Manager
Puget Sound Energy —Bothell, WA
- $82,000 - $136,300 a year
- 5 years
- Analysis skills
- Accounting
- AD&D insurance
- Paid holidays
Regulatory Affairs Associate/Senior Regulatory Affairs Associate
Fred Hutchinson Cancer Center —Seattle, WA
- $80,172 - $146,681 a year
- Full-time
- Mid-level
- Bachelor's degree
- Continuous improvement
- Paid parental leave
- Paid holidays
Regulatory Affairs Specialist II
Seattle Children's Hospital —Seattle, WA
- $80,715 - $121,073 a year
- Master's degree
- Bachelor's degree
- Pediatrics
- Health insurance
- Dental insurance
7d
Director, Regulatory Compliance
Premera Blue Cross —Mountlake Terrace, WA
- $157,900 - $315,900 a year
- Online Application
- Supervising experience
- Bachelor's degree
- Experience equivalent to degree accepted
- Free parking
- Wellness program
Regulatory Affairs Consultant, In Silico Modeling
Pharmatech Associates —Seattle, WA
- Part-time
- Senior level
- Leadership
- 10 years
Trade Policy Analyst
Bryant Christie Inc. —Seattle, WA
- $75,000 - $85,000 a year
- Full-time
- Hybrid work
- Writing skills
- Mid-level
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
8h
Regulatory Coordinator I/II - Lab Based Studies
Fred Hutchinson Cancer Center —Seattle, WA
- $28.36 - $50.12 an hour
- Full-time
- Hybrid work
- Mid-level
- High school diploma or GED
- Associate's degree
- Paid parental leave
- Paid holidays
Associate Director / Director, Regulatory Affairs – IHC Companion Diagnostics (CDx)
SystImmune —Redmond, WA
- $150,000 - $230,000 a year
- Full-time
- Office
- Bachelor's degree
- Mentoring
- Paid holidays
- Disability insurance
Strategic Researcher
WSNA —Tukwila, WA
- $89,635.10 - $169,738.61 a year
- Full-time
- Microsoft Excel
- Office
- Analysis skills
- Paid holidays
- Health insurance
Quick Apply
Medical Device Regulatory Affairs & Clinical Evaluation Manager
Global Regulatory Writing & Consulting (GLOBAL) —Bellevue, WA
- Full-time
- Microsoft Excel
- 5 years
- English
Scientist/Senior Scientist, Companion Diagnostics (CDx) – IHC Development
SystImmune —Redmond, WA
- $90,000 - $140,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
- Paid holidays
- Disability insurance
Dir, Clinical Research Quality Assurance and Regulatory Support
Seattle Children's Hospital —Seattle, WA
- $180,884 - $271,326 a year
- 7 years
- Master's degree
- Bachelor's degree
- Health insurance
- Dental insurance
Health Sciences Research Coordinator
Veteran Affairs —Seattle, WA
- $69,000 - $76,000 a year
- Email
- Microsoft Excel
- Microsoft Outlook
- Customer service
- Health insurance
- Dental insurance
Quick Apply
Senior Clinical Trial Manager
Umoja Biopharma —Seattle, WA
- $125,000 - $175,000 a year
- Office
- Bachelor's degree
- Travel
- Commuter assistance
- Health insurance
Quick Apply

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Clinical Research Coordinator II - Experienced | Rheumatology Research

Confidential -
Bellevue, WA

Quick Apply

Job Details

Full-time
$32 - $36 an hour

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance

Qualifications

Clinical research
Medical software
Bachelor's degree in biology
Medical research
Bachelor's degree
Healthcare research

Full Job Description

This position is on-site, and you must live in WA state.

Clinical Research Coordinator - Experienced | Rheumatology Research

NO RELOCATION AVAILABLE - OPEN TO CANDIDATES RESIDING IN THE SEATTLE AREA

Pay: Range of $32 to $36/hour

Job description:

A growing rheumatology-focused clinical research program is seeking a full-time Clinical Research Coordinator (CRC). This role supports the advancement of research in rheumatologic diseases and works closely with the Clinical Research Manager and Principal/Sub-Investigators to facilitate industry-sponsored clinical trials.

We are particularly interested in candidates who are highly motivated, quick learners, and currently working as Clinical Research Coordinators, with strong patient interaction experience and familiarity with CRIO and other clinical research systems.

The Clinical Research Coordinator will:

Ensure the study specific informed consent is signed by the subjects or the caregivers.
Code, evaluate, or interpret collected study data.
Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
Communicate with laboratories or investigators regarding laboratory findings.
Solicit industry-sponsored trials through contacts and professional organizations.
Order drugs or devices necessary for study completion.
Direct the requisition, collection, labeling, storage, or shipment of specimens.
Arrange research study sites and determine staff or equipment availability.
Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues.
Register protocol patients with appropriate statistical centers as required.
Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
Perform specific protocol procedures such as taking vital signs and performing electrocardiograms.
Prepare lab samples for overnight shipment, including handling of dry ice (prefer IATA certification).
Interpret protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics.
Develop advertising and other informational materials to be used in subject recruitment.
Contact industry representatives to ensure equipment and software specifications necessary for successful study completion.
Confer with health care professionals to determine the best recruitment practices for studies.
Organize space for study equipment and supplies.
Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.
Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, and potential subject risks.
Record adverse events and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
Prepare study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports.
Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data.
Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.
Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts such as protocol revisions.
Dispense medical devices or drugs and calculate dosages and provide instructions as necessary.
Contact outside health care providers and communicate with subjects to obtain follow-up information.
Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.
Schedule subjects for appointments and procedures as required by study protocols, and ensure subject compliance with visit attendance.
Bonus skills: Thorough knowledge of CRIO and EDC.

Additional Requirements:

Bachelor's degree in biology
Interest in continuing with research as a career path.
Must be willing to commit to at least 2 years and have at least 1 year of clinical research experience in the US.
Must have vaccinations in accordance with CDC guidelines in addition to completed COVID vaccination series.

Job Type: Full-time

Benefits:

401(k)
Dental insurance
Health insurance
Paid time off
Vision insurance

Medical Specialty:

Rheumatology

Application Question(s):

Does the salary listed meet your expectations?
This position is on-site, and you must live in WA state prior to accepting this position if offered. Do you reside in WA state?

Education:

Bachelor's (Required)

Experience:

Clinical research: 1 year (Required)
Work Location: In person

Pay: $32.00 - $36.00 per hour

Benefits:

401(k)
Dental insurance
Health insurance
Paid time off

Application Question(s):

Must be willing to commit to at least 2 years and have at least 1 year of clinical research experience in the US.
Does the salary OF $35/hr listed meet your expectations?
This position is on-site, and you must live in WA state prior to interviewing for this position. Do you reside in WA state? This is required to move forward with the interview process.

Education:

Bachelor's (Required)

Experience:

Clinical research: 1 year (Required)
Thorough knowledge of CRIO and EDC.: 1 year (Required)

Location:

Bellevue, WA 98004 (Preferred)

Work Location: In person

Quick Apply

Refine Your Search

regulatory affairs jobs in bothell wa

Clinical Research Coordinator II - Experienced | Rheumatology Research

Director of Regulatory Compliance-Oral Healthcare

Senior Regulatory Affairs Specialist

Medical Science Liaison, Oncology (Northern CA, OR, WA, MT, ID)

Post Market Surveillance Specialist

Post Market Surveillance (PMS) Specialist

Economic Development Manager

Regulatory Affairs Associate/Senior Regulatory Affairs Associate

Regulatory Affairs Specialist II

Director, Regulatory Compliance

Regulatory Affairs Consultant, In Silico Modeling

Trade Policy Analyst

Regulatory Coordinator I/II - Lab Based Studies

Associate Director / Director, Regulatory Affairs – IHC Companion Diagnostics (CDx)

Strategic Researcher

Medical Device Regulatory Affairs & Clinical Evaluation Manager

Scientist/Senior Scientist, Companion Diagnostics (CDx) – IHC Development

Dir, Clinical Research Quality Assurance and Regulatory Support

Health Sciences Research Coordinator

Senior Clinical Trial Manager

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