Clinical Research Coordinator - Multi-Site Trials & Patient Care

Alcanza Clinical Research; Katy (TX); On-site; USD 42,000 - 72,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401k with safe harbor match

Short/long-term disability and life保险

Job summary

Alcanza Clinical Research in Katy, TX seeks a Clinical Research Coordinator to ensure compliant execution of assigned studies. You will collaborate with site team to screen participants, obtain consent, and collect data per GCP and SOPs.

The role requires a Medical Assistant diploma or equivalent with 1+ year in clinical research or clinical practice, and preferred bilingual English/Spanish communication.

Qualifications

• Medical Assistant diploma or equivalent plus 1 year of clinical research/clinical experience
• Proficiency in basic clinical procedures (blood pressure, vitals, EKGs, phlebotomy)
• Bi-lingual English/Spanish preferred

Responsibilities

• Screen patients for study enrollment
• Obtain informed consent from patients
• Document data in source charts and EDC; manage vital signs and ECGs
• Maintain confidentiality and HIPAA compliance

Skills

Bilingual English/Spanish

Organizational skills

Communication skills

Education

Medical Assistant diploma

LPN/LVN

EMT credential

Associate’s degree

Tools

Microsoft Office

Electronic Health Records

Job description

Alcanza Clinical Research in Katy, TX seeks a Clinical Research Coordinator to ensure compliant execution of assigned studies. You will collaborate with site team to screen participants, obtain consent, and collect data per GCP and SOPs.

The role requires a Medical Assistant diploma or equivalent with 1+ year in clinical research or clinical practice, and preferred bilingual English/Spanish communication.