Clinical Research Coordinator

Activian Clinical Research; Houston (TX); On-site; USD 55,000 - 75,000; Full time

Job summary

Activian Clinical Research in the Greater Houston area is seeking an experienced Clinical Research Coordinator for a full-time, on-site role. You will coordinate and implement studies, ensure compliance with GCP, regulatory requirements, and protocols, and support study visits and patient enrollment.

The ideal candidate has at least 2 years of CRC experience, strong communication and organizational skills, and is comfortable traveling between Houston-area sites.

Qualifications

• Minimum 2 years of experience as a Clinical Research Coordinator.
• Strong knowledge of GCP, informed consent procedures and protocol compliance.
• Experience managing trials across multiple phases and indications.
• Excellent communication, organizational and interpersonal skills.
• Detail-oriented, self-motivated and able to work independently or in a team.
• Proficiency in clinical trial software and electronic data capture systems.
• Willing to travel between sites within the Greater Houston area.

Responsibilities

• Coordinate and manage day-to-day activities of clinical research studies.
• Recruit, screen, and enroll study participants.
• Obtain and document informed consent.
• Ensure adherence to study protocols and regulatory guidelines.
• Maintain accurate study records and documentation.
• Liaise with investigators, clinical staff, CROs, and sponsors.
• Blood draws and lab processing when necessary.
• Support all aspects of study visits and follow-up procedures.

Skills

Communication

Organization

Interpersonal skills

Attention to detail

Independent / team player

Tools

EDC software

Clinical trial software

Job description

We are seeking an experienced and highly motivated Clinical Research Coordinator (CRC) to join our team in the Greater Houston area. In this full-time, on-site role, the CRC will be responsible for the coordination and implementation of clinical research studies, ensuring studies are conducted in compliance with Good Clinical Practice (GCP), regulatory requirements, study protocols, and institutional policies. We are quickly expanding our presence in the Houston area and are looking for a CRC with phlebotomy experience and someone open to traveling to different sites!

Key Responsibilities:

• Coordinate and manage day-to-day activities of clinical research studies
• Recruit, screen, and enroll study participants
• Obtain and document informed consent
• Ensure strict adherence to study protocols and regulatory guidelines
• Maintain accurate and up-to-date study records and documentation
• Liaise with investigators, clinical staff, CROs, and sponsors
• Blood draws and lab processing when necessary
• Support all aspects of study visits and follow-up procedures

Qualifications:

• Minimum of 2 years of experience as a Clinical Research Coordinator
• Strong knowledge of GCP, Informed Consent procedures, and Protocol compliance
• Previous experience managing clinical trials across various phases and indications
• Excellent communication, organizational, and interpersonal skills
• Highly detail-oriented, self-motivated, and capable of working independently or as part of a team
• Proficiency in clinical trial software and electronic data capture systems
• Comfortable working in a fast-paced clinical setting
• Willingness to float between sites in the Greater Houston area
• Bilingual (English/Spanish) preferred but not required