Clinical Research Coordinator — In-Person, Training Provided

No Resistance Consulting Group; San Diego (CA); On-site; USD 31,000 - 34,000; Full time

Benefits offered by this job

401(k)

Dental Insurance

Health Insurance

Paid time off

Vision Insurance

Job summary

No Resistance, a clinical trial site management organization, is seeking motivated individuals for in-person, full-time roles in San Diego. The position involves executing clinical research projects with focus on safety, data integrity, and regulatory compliance.

Expect regular hours Monday–Friday, with a 40-hour workweek in a clinical setting. You will recruit, consent, collect samples, and ensure high-quality data while working closely with a clinical team.

Qualifications

• Ability to work independently in a clinical setting.
• Genuine interest in clinical research and patient-facing work.
• Excellent attention to detail and meticulous data handling.
• Timely, clear communication with team and stakeholders.

Responsibilities

• Maintain regulatory binders and inventory for study supplies.
• Recruit and enroll study subjects.
• Obtain informed consent from participants.
• Collect nasal swab samples and process for testing.
• Test samples on investigational PCR analyzers.
• Enter data and perform data quality checks.
• Resolve data queries and ensure protocol compliance.
• Organize clinical work areas and manage shipment of materials.

Skills

Independent work

Attention to detail

Patient interaction

Timely communication

Job description

No Resistance, a clinical trial site management organization, is seeking motivated individuals for in-person, full-time roles in San Diego. The position involves executing clinical research projects with focus on safety, data integrity, and regulatory compliance.

Expect regular hours Monday–Friday, with a 40-hour workweek in a clinical setting. You will recruit, consent, collect samples, and ensure high-quality data while working closely with a clinical team.