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Open nowPosted yesterday

Clinical Research Coordinator Associate

Stanford372 open roles

Where
Stanford, CA, United States
Work mode
Hybrid
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Your applicationOpen nowClinical Research Coordinator AssociateStanford · Stanford, CA, United States

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The clock on this job

Early applications get read.

8.3% of postings close within 7 days. Measured by our own scanner across the market. Stanford postings stay open a median of 4 days.

Share of postings closed within
  1. 1.9%1 day
  2. 3.9%3 days
  3. 8.3%7 days
  4. 15.3%14 days
  5. 34.2%30 days
This job: posted yesterday

Stanford median: 4 days open

The posting

Job Description

We are seeking a superstar, highly motivated, organized, reliable, and community-oriented English/Spanish bilingual Full-Time Research Coordinator / Research Data Collector for a Stanford family healthy weight research program for children with obesity and their parents.

The research study includes weekly family-based group sessions, online activities, and repeated research assessments over time. This position will serve as a primary data collector for child and parent assessments, including administering surveys and physical measurements and will also support weekly family sessions.

Some evening and/or weekend availability will be required.

Duties include:

  • Coordinate study activities from startup through close-out, including participant recruitment, screening, scheduling, enrollment, data collection, and follow-up.
  • Serve as a primary contact for research participants, families, sponsors, regulatory agencies, and community partners.
  • Communicate regularly with prospective and enrolled families in a professional, supportive, and culturally appropriate manner.
  • Determine participant eligibility, obtain informed consent according to protocol, and assist with recruitment and community outreach strategies.
  • Serve as a primary data collector for child and parent assessments, including administering surveys, questionnaires, and standardized interview questions.
  • Explain study procedures to participants in a clear, professional, and participant-friendly manner.
  • Collect child and parent study data according to standardized research protocols, study manuals, and certification requirements.
  • Conduct anthropometric and related body composition measurements, including height, weight, waist circumference, and other study-specified measures.
  • Coordinate and administer health behavior assessments, including physical activity, sedentary behavior, sleep, screen time, and dietary assessment procedures.
  • Enter, manage, and track participant data in secure study databases accurately and promptly.
  • Develop and maintain study-related documents, flow sheets, case report forms, tracking logs, and other study materials.
  • Review study records and case report forms for completeness and accuracy against source documents.
  • Track assessment completion, coordinate reminders and make-up visits, and proactively follow up with families to minimize missing data.
  • Ensure compliance with research protocols, institutional requirements, IRB approvals, and regulatory documentation standards.
  • Prepare regulatory submissions and assist with IRB renewals, monitor visits, sponsor meetings, and regulatory audits.
  • Interact regularly with the principal investigator and study team to ensure participant safety, data quality, and adherence to proper study conduct.
  • Assist with training and supervision of additional study staff related to recruitment, enrollment, assessment procedures, and data collection.
  • Participate in delivery of weekly group health behavior change sessions for children and parents during evening hours.
  • Participate in family engagement and participation throughout the intervention program.

* - Other activities as needed to assist in the successful conduct of the study.

Responsibilities

Core Duties:

  • Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through closeout.
  • Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies.
  • Coordinate collection of study specimens and processing.
  • Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms.
  • Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions and ensure Institutional Review Board renewals are completed.
  • Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
  • Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.
  • Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.
  • Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
  • Participate in monitor visits and regulatory audits.

Minimum Education and Experience

Two-year college degree and two years related work experience or a bachelor’s degree in a related field or an equivalent combination of related education and relevant experience.

Knowledge, Skills and Abilities:

  • Strong interpersonal skills.
  • Proficiency with Microsoft Office.
  • Knowledge of medical terminology.

Certificates and Licenses Required

Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.

Qualifications

[REMOVE STATEMENT BEFORE POSTING - KEEP LANGUAGE BELOW, IF APPLICABLE. REMOVE IF NOT APPLICABLE]

Drivers License Requirements

  • Must possess and maintain a valid California non-commercial Class C Driver's License.
  • Ability to drive day or night.
  • When conducting university business, must comply with the California Vehicle Code and Stanford University driving requirements.
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