IRB/FDA-Regulated Clinical Research Coordinator

Alaka`ina Foundation Family of Companies; San Antonio (TX); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

401K plan with company match

medical, dental, disability, and life

tuition reimbursement

paid time off

11 paid holidays

Job summary

Bering-Alaka`ina Holdings, LLC is seeking a Clinical Research Coordinator to support government projects in San Antonio, TX. You will coordinate human studies, ensure timelines and study designs are followed, and oversee regulatory documentation under ICH and FDA guidelines.

The role requires a biological sciences degree and active CITI/GCP training, with responsibilities spanning enrollment, data management, and cross-functional communication with investigators and staff.

Qualifications

• Must provide proof of immunization or immunity per DHA guidelines.
• CITI certifications must be completed and GCP applied in research operations.
• Willing to sign a Non-Disclosure Agreement (NDA).

Responsibilities

• Serve as primary coordinator for execution of human research studies and timelines.
• Coordinate multiple projects ensuring progression and adherence to protocols.
• Provide training to research staff on laboratory techniques and clinical contact protocols.
• Develop comprehensive study schedules and coordinate activities among participants, lab staff, and the PI.
• Assist with participant enrollment and ensure recruitment aligns with approved protocols.
• Maintain accurate study records and provide follow-up documentation to the PI.
• Ensure participant safety and protocol compliance per ICH guidelines.
• Organize research data lifecycle and prepare reports and publications submissions.

Skills

GCP training

Immunization compliance

NDA readiness

Education

Bachelor's degree in biological sciences

Job description

Bering-Alaka`ina Holdings, LLC is seeking a Clinical Research Coordinator to support government projects in San Antonio, TX. You will coordinate human studies, ensure timelines and study designs are followed, and oversee regulatory documentation under ICH and FDA guidelines.

The role requires a biological sciences degree and active CITI/GCP training, with responsibilities spanning enrollment, data management, and cross-functional communication with investigators and staff.