Onsite Clinical Research Coordinator — Phase 2-4 Trials, Strong Benefits

Infusion PA; San Antonio (TX); On-site; USD 43,000 - 48,000; Full time

Benefits offered by this job

PTO buy-back

PTO rollover

PTO donation program

Wellness reimbursement program

Tuition assistance and professional91

Job summary

Vivo Infusion is seeking a detail-oriented Clinical Research Coordinator in San Antonio, TX, to oversee daily activities across phase 2-4 pharmaceutical trials. The onsite role requires 1 year of clinical research experience, strong organization, and the ability to manage multiple protocols with accuracy.

Workweek is Monday to Friday, 8:00am–5:00pm. The team emphasizes patient care, protocol adherence, and collaboration with investigators and site staff.

Qualifications

• 1 year of working experience in clinical research, required.
• Extremely detail-oriented with exceptional organizational skills, required.
• Highly self-motivated with the ability to manage tasks independently or as part of a dynamic team.
• Ability to manage a variety of protocols and tasks simultaneously with accuracy.

Responsibilities

• Conduct site feasibility and review study protocols to ensure compatibility and compliance.
• Recruit and screen patients for clinical trials, ensuring adherence to eligibility criteria.
• Facilitate the informed consent process, ensuring participants fully understand the study.
• Study procedure coordination, including treatment administration as applicable.
• Maintain accountability for investigational product (IP) management, as applicable.
• Collect and enter data into case report forms, addressing and working to resolve any queries.
• Actively participate in investigator meetings. Participate and assist with site initiation, monitoring, and close-out visits.

Skills

Clinical research experience

Detail-oriented

Organizational skills

Self-motivation

Multi-tasking

Education

Associate degree or higher (healthcare/medical)

High school diploma or equivalent

Job description

Vivo Infusion is seeking a detail-oriented Clinical Research Coordinator in San Antonio, TX, to oversee daily activities across phase 2-4 pharmaceutical trials. The onsite role requires 1 year of clinical research experience, strong organization, and the ability to manage multiple protocols with accuracy.

Workweek is Monday to Friday, 8:00am–5:00pm. The team emphasizes patient care, protocol adherence, and collaboration with investigators and site staff.