Clinical Trials Coordinator — Patient-Centric Research

MD Ally; Port Arthur (TX); On-site; USD 50,000 - 65,000; Full time

Job summary

MD Ally in Port Arthur, Texas, seeks a Clinical Research Coordinator to manage industry-sponsored clinical trials. Responsibilities include leading patient recruitment, conducting visits, and maintaining study documentation.

The ideal candidate has 1-2 years of clinical research experience and a degree in a related field. Strong communication skills and the ability to work with diverse teams are essential.

MD Ally is committed to creating an inclusive workplace.

Qualifications

• Minimum 1-2 years of clinical research experience.
• Must be able to lift up to 25 pounds.

Responsibilities

• Manage industry-sponsored clinical trials and conduct patient visits.
• Handle patient recruitment and schedule research visits.
• Maintain communication with all study stakeholders.

Skills

Strong written and verbal communication skills

Ability to execute on research tasks

Ability to read and apply clinic policies

Ability to use standard office software

Education

Medical Assistant, LPN, Associates or Bachelor’s degree

Job description

MD Ally in Port Arthur, Texas, seeks a Clinical Research Coordinator to manage industry-sponsored clinical trials. Responsibilities include leading patient recruitment, conducting visits, and maintaining study documentation.

The ideal candidate has 1-2 years of clinical research experience and a degree in a related field. Strong communication skills and the ability to work with diverse teams are essential.

MD Ally is committed to creating an inclusive workplace.