Clinical Research Coordinator I - Trials & Patient Care

CARUM RESEARCH INC; Dallas (TX); On-site; USD 48,000 - 65,000; Full time

Job summary

CARUM RESEARCH INC. in Dallas, TX seeks a Clinical Research Coordinator (CRC) to manage trials, review protocols, and ensure SOP compliance.

The role involves data entry, coordinating with sponsors, IRB, and CROs, plus ongoing training in good clinical practice. Responsibilities include participant visits (in-person/virtual), document development, regulatory submissions, and safeguarding study confidentiality while ensuring ethical standards are met.

Qualifications

• High School Diploma or GED with 3 years health care, customer service, or administrative support experience.
• Two years of college in a scientific, health-related, or business program and one year of related health care, customer service, or administrative experience.
• Licensed as an LPN/LVN with one year of related experience.
• Bachelor's or higher in a scientific, health-related, or business field.

Responsibilities

• Communicates with study investigators, sponsors, IRB, and others about protocols and recruitment.
• Assists in recruitment strategy development and participant screening.
• Conducts in-person, virtual, or telephone-based study visits.
• Reviews records, attends recruitment events, and interacts with participants.
• Develops flow sheets and source documents for the study.
• Maintains accurate study documents and audits CRFs against source data.
• Implements IRB-approved protocol changes to visits and documentation.
• Participates in sponsor webinars, teleconferences, and investigator meetings.

Skills

Attention to detail

Teamwork

Multi-tasking

Communication

Customer service

Education

High School Diploma or GED

Two years of college in scientific/health/business + 1 year related experience

LPN/LVN license

Bachelor's/Master/MD/PhD in science/health/business

Job description

CARUM RESEARCH INC. in Dallas, TX seeks a Clinical Research Coordinator (CRC) to manage trials, review protocols, and ensure SOP compliance.

The role involves data entry, coordinating with sponsors, IRB, and CROs, plus ongoing training in good clinical practice. Responsibilities include participant visits (in-person/virtual), document development, regulatory submissions, and safeguarding study confidentiality while ensuring ethical standards are met.