Onsite Clinical Research Coordinator – San Antonio

National Institute of Clinical Research, Inc.; San Antonio (TX); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Medical, Dental, and Vision Insurance

401(k) with company match

Paid Time Off (PTO)

Job summary

The National Institute of Clinical Research (NICR) seeks a Clinical Research Coordinator to oversee studies from initiation through final report, onsite in San Antonio, TX. The CRC will ensure quality, compliance, and efficiency in trial conduct.

Responsibilities include coordinating visits, monitoring enrollment, maintaining GCP/ICH compliance, and collaborating with investigators, sponsors, and staff. Travel to Hesperia and Barstow may be required.

Qualifications

• Minimum of 2 years of clinical research experience.
• Knowledge of GCP and ICH guidelines.
• Strong interpersonal and communication skills.
• Excellent organizational and planning abilities.
• Willing to travel to Hesperia and Barstow.
• Local to San Antonio, TX area; onsite/full-time position.

Responsibilities

• Manage clinical studies from initiation through closeout.
• Oversee daily trial operations to ensure protocol adherence and data integrity.
• Maintain regulatory compliance with GCP and ICH guidelines.
• Coordinate study visits, track enrollment, and ensure accurate documentation.
• Anticipate and coordinate study needs proactively.
• Collaborate with investigators, sponsors, and clinical staff to support trial success.

Job description

The National Institute of Clinical Research (NICR) seeks a Clinical Research Coordinator to oversee studies from initiation through final report, onsite in San Antonio, TX. The CRC will ensure quality, compliance, and efficiency in trial conduct.

Responsibilities include coordinating visits, monitoring enrollment, maintaining GCP/ICH compliance, and collaborating with investigators, sponsors, and staff. Travel to Hesperia and Barstow may be required.