Clinical Research Assistant- Irvine, CA (On Site)

Gilder Search Group; Irvine (CA); On-site; USD 85,962,000 - 114,616,000; Full time

Job summary

Gilder Search Group seeks a Clinical Research Assistant in Irvine, CA, to accurately measure blood pressure via auscultatory methods, follow GCP/HIPAA standards, and support participant recruitment and study documentation. The role is a 40-hour per week, in-person contract through year-end with potential extension.

Responsibilities include coordinating with the PI and cross-functional teams, data entry and quality checks, and preparing progress reports while maintaining study supplies.

Qualifications

• Hands-on experience as a clinical research assistant or similar role, including recruitment and enrollment
• Medical-related or science degree preferred but not required if experience is sufficient

Responsibilities

• Accurately measure and record blood pressure using auscultatory methods as part of study procedures
• Coordinate with Principal Investigator and cross-functional teams to follow research protocols
• Support recruitment and enrollment of study participants, including scheduling and logistics
• Organize and maintain study documents with data entry and quality control
• Assist in preparing detailed reports on study progress and findings
• Maintain clinical supplies for the study

Skills

Blood pressure measurement

GCP

HIPAA

Independent work

Communication skills

Organization

Education

Medical/science degree preferred

Job description

POSITION SUMMARY

We are seeking a Clinical Research Assistant with hands-on experience in accurately measuring blood pressure using auscultatory method, following clinical standards and best practices. This skill is essential for study activities and will be a key responsibility in this role.

The candidate with support the implementation of human research study activities sponsored by our client, in accordance with the approved protocols, applicable regulatory regulations and GCP guidelines. The candidate will work closely with multidisciplinary team members to facilitate activities related to one or more research projects.

MAJOR RESPONSIBILITIES

*This list is not all inclusive. Additional duties will be assigned as needed.

• Accurately measure and record blood pressure using auscultatory methods as part of study procedures
• Work with the Principal Investigator and cross-functional teams to facilitate daily activities and comply with research protocols
• Supports the recruitment and enrollment of study participants, including coordinating visit schedules and assisting with logistical arrangements
• Organization and maintenance of all research study documents including data entry, routine data verification and quality control
• Assists in preparation of detailed reports surrounding study, study progress and findings
• Maintain clinical supplies for the study assign

KNOWLEDGE, SKILLS, AND ABILITIES

• Competency in taking blood pressure using auscultatory methods, following clinical standards and best practices
• Understanding of Good Clinical Practice (GCP), and HIPAA regulations
• Ability to work independently and collaboratively with minimal supervision, and adapt to changing priorities
• Excellent interpersonal, verbal, and written communication skills
• Strong organizational and time management skills

EDUCATION & EXPERIENCE

• Prior hands-on experience in a clinical research assistant or similar role is required, including direct involvement in participant recruitment and enrollment
• A degree in a medical-related or science field is preferred but not required if the candidate demonstrates sufficient experience and competence in performing study-related tasks.

Contract: Until the end of the year with possible extension

Hours approximately: 40

Location: Irvine, CA

Job Types: Full-time, Contract

Hourly Rate: $30-$40 hourly

Schedule: 8 hour shift

Work Location: In person