Clinical Research Coordinator

Activian Clinical Research; Tomball (TX); On-site; USD 48,000 - 78,000; Full time

Job summary

Activian Clinical Research in the Greater Houston area seeks an experienced Clinical Research Coordinator for a full-time, on-site position. Primary site is Tomball, with travel to other Houston-area sites as needed, and phlebotomy experience preferred.

You will coordinate studies, recruit participants, obtain informed consent, ensure GCP compliance, maintain study records, and liaise with investigators, CROs, and sponsors to support visits and follow-ups.

Qualifications

• Minimum 2 years as a Clinical Research Coordinator.
• Strong knowledge of GCP and informed consent procedures.
• Experience across clinical trial phases and indications.
• Excellent communication and organizational skills.
• Ability to work independently or in a team.

Responsibilities

• Coordinate day-to-day activities of studies.
• Recruit, screen and enroll participants.
• Obtain and document informed consent.
• Ensure protocol and regulatory compliance.
• Maintain study records and documentation.
• Liaise with investigators, CROs, sponsors.
• Blood draws and lab processing shipping.
• Support study visits and follow-up.

Skills

GCP knowledge

Informed consent

Study coordination

EDC software

Communication

Organization

Tools

EDC 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! For this role, our Tomball site will be the primary location, but the candidate must be open to traveling to different sites in the Houston area, when needed.

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, lab processing shipping
• 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