Pulmonary Clinical Research Coordinator II – Spanish Preferred
Seattle Children's
full-time
Posted on:
Location Type: Office
Location: Seattle • Washington • 🇺🇸 United States
Visit company websiteSalary
💰 $35 - $53 per hour
Job Level
JuniorMid-Level
Tech Stack
Google Cloud Platform
About the role
- Assist with the identification, screening, and enrollment of eligible subjects for clinical research studies via telephone and/or in-person interactions
- Conduct study visits according to established protocols, ensuring a positive and comfortable experience for participants
- Support the accurate administration of questionnaires, diaries, and other data collection instruments as required by study protocols
- Assist in the thorough review of study documents (e.g., consent forms, case report forms) to ensure completeness, accuracy, and strict adherence to regulatory guidelines (e.g., GCP, HIPAA)
- Perform accurate and timely data entry into various study databases and contribute to ongoing efforts to ensure data integrity and consistency across all research records
- Maintain a professional, empathetic, and compassionate demeanor when interacting with patients, ensuring their comfort and understanding throughout their participation
- Perform other related duties to support the overall goals of the research initiative
Requirements
- Bachelor's degree in a health-related field (e.g., Nursing, Biology, Public Health) or equivalent experience
- Previous experience in clinical research, particularly involving patient interaction and biological sample collection, is highly preferred
- Fluency in Spanish (both verbal and written) is strongly preferred
- Exceptional attention to detail and a commitment to maintaining precise and accurate records
- Strong organizational skills and the ability to manage multiple tasks effectively in a fast-paced environment
- Excellent written and verbal communication skills
- Proficiency with Microsoft Office Suite (Word, Excel, Outlook) and experience with electronic data capture (EDC) systems is a plus
- Knowledge of Good Clinical Practice (GCP) guidelines and human subject protection regulations (e.g., IRB)
- Ability to work independently and collaboratively as part of a team
Benefits
- Medical, dental, and vision plans
- 403(b)
- Life insurance
- Paid time off
- Tuition reimbursement
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
data entrydata collectionbiological sample collectionclinical researchattention to detailrecord keepingprotocol adherencedata integritySpanish fluency
Soft skills
empathycommunicationorganizational skillsteam collaborationindependencemultitaskingpatient interaction