Clinical Research Coordinator

Epic Medical Research, LLC.; DeSoto (TX); Sur place; USD 52 000 - 74 000; Plein temps

Résumé du poste

Epic Medical Research, LLC. is seeking a Clinical Research Coordinator for our DeSoto, TX site.

The role involves managing day-to-day trial activities, participant recruitment, screening, and enrollment, as well as coordinating visits and follow-up. It requires maintaining regulatory compliance, data integrity, and collaboration with investigators and sponsors.

Qualifications

• Experience with clinical trials and site coordination
• Proficiency in informed consent processes and participant education
• Understanding of study protocol implementation and research best practices
• Experience with data collection, documentation, and regulatory standards
• Knowledge of GCP, HIPAA, and FDA/ICH guidelines is a plus
• Strong organizational, time management, and attention-to-detail abilities
• Excellent interpersonal and communication skills with participants and sponsors
• Ability to work on-site in DeSoto, TX and manage multiple studies

Responsabilités

• Manage day-to-day conduct of clinical trials at the DeSoto site.
• Recruit, screen, and enroll study participants.
• Coordinate study visits and follow-up activities.
• Obtain and document informed consent; ensure protocol adherence.
• Maintain source documents and case report forms; support regulatory tasks.
• Collaborate with investigators, sponsors, and site staff for data quality.
• Monitor participant safety and report adverse events.
• Support site operations and process improvements.

Connaissances

Clinical research experience

Informed consent

Protocol adherence

Data collection & documentation

Strong communication

Organizational skills

Time management

Attention to detail

Interpersonal skills

Formation

Bachelor’s degree in health-related or scientific field

Description du poste

Company Description

Epic Medical Research collaborates with sponsors to accelerate the development and delivery of new therapies through rigorous science and data-driven solutions. The organization operates clinical trial sites across Alabama, Arizona, California, Florida, Louisiana, Oklahoma, and Texas, providing broad access to diverse patient populations. A skilled multidisciplinary team uses advanced research methodologies and analytics to examine social, cultural, and biological factors that influence health outcomes. This approach supports the generation of robust, high-quality data that drives effective treatment development. As a trusted partner in healthcare innovation, Epic Medical Research is committed to improving health and well-being in diverse communities nationwide.

Role Description

This full-time, on-site Clinical Research Coordinator role is based in DeSoto, TX. The Clinical Research Coordinator will manage the day-to-day conduct of clinical trials, including participant recruitment, screening, and enrollment, as well as coordination of study visits and follow-up. Responsibilities include obtaining and documenting informed consent, ensuring adherence to study protocols, maintaining accurate source documents and case report forms, and supporting regulatory and compliance activities. The role involves close collaboration with investigators, sponsors, and site staff to ensure timely data collection, query resolution, and overall study quality. The Clinical Research Coordinator will also help monitor participant safety, report adverse events, and support continuous improvement of site operations.

Qualifications

• Candidates should possess strong clinical research experience and hands-on involvement with clinical trials.


• Candidates should possess skills in informed consent processes and participant education regarding study requirements and risks.


• Candidates should possess a solid understanding of study protocol implementation and research best practices.


• Candidates should possess experience with data collection, documentation, and adherence to regulatory and ethical standards.


• Bachelor’s degree in a health-related or scientific field (or equivalent experience) preferred.


• Knowledge of Good Clinical Practice (GCP), HIPAA, and FDA/ICH guidelines beneficial.


• Strong organizational, time management, and attention-to-detail skills, with the ability to manage multiple studies or tasks.


• Effective interpersonal and communication skills for working with participants, investigators, and sponsor representatives.


• Ability to work on-site in DeSoto, TX, and maintain professionalism in a fast-paced clinical environment.


• Prior experience in outpatient research sites or similar clinical settings is an advantage.