Advanced Clinical Research Coordinator

RiseMe; Dallas (TX); On-site; USD 60,000 - 76,000; Full time

Benefits offered by this job

PPO medical plan

Paid Time Off

Retirement Programs

Paid Parental Leave

Tuition Reimbursement

Job summary

UT Southwestern in Dallas seeks a Clinical Research Coordinator to support investigators by coordinating patient participation and data collection across multiple studies. The role requires ensuring protocol adherence, regulatory compliance, and data integrity with training and oversight from the PI.

The position involves interactions with participants via in-person or telehealth visits, with responsibilities including budgeting assistance, safety monitoring, and assisting in IRB submissions as

Qualifications

• Bachelor's degree in medical or science field is required.
• Minimum 2 years of clinical research experience.
• Licenses and Certifications: BLS, CPR AED; ACRP or SOCRA certification preferred.

Responsibilities

• Coordinate regulatory documentation to comply with FDA, HRPP and university policies.
• Screen, recruit, enroll and follow subjects per study protocol.
• Develop and manage data collection tools and case report forms (CRFs).
• Assist in protocol development and budget preparation for studies.
• Monitor patient safety and assist with research billing and calendars.

Skills

Clinical research coordination

Regulatory documentation

Data management

Education

Bachelor's degree in medical or science related field

Job description

UT Southwestern in Dallas seeks a Clinical Research Coordinator to support investigators by coordinating patient participation and data collection across multiple studies. The role requires ensuring protocol adherence, regulatory compliance, and data integrity with training and oversight from the PI.

The position involves interactions with participants via in-person or telehealth visits, with responsibilities including budgeting assistance, safety monitoring, and assisting in IRB submissions as