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**Job Title**: Clinical Research Coordinator
**Location**: Houston, Texas
**Company**: Clinical Trial Network llc
**Position Type**: Full-time
**Visa**: TN offered
We are seeking a highly motivated, organized, and experienced Clinical Research Coordinator to join our team. As a Clinical Research Coordinator, you will play a critical role in the planning, implementation, and coordination of clinical research studies conducted within Clinical Trial Network.
**Responsibilities**:
1. Coordinate and manage all aspects of clinical research studies, including participant recruitment, enrollment, and follow-up.
2. Ensure compliance with regulatory requirements, including obtaining informed consent, adherence to study protocols, and maintaining accurate and complete study documentation.
3. Collaborate with principal investigators, study sponsors, and other stakeholders to develop study protocols and research objectives.
4. Schedule and conduct study visits, collect and process study-related data, and ensure timely and accurate data entry into study databases.
5. Monitor participant safety and adverse events throughout the course of the study, and report any concerns or deviations from protocol to the appropriate parties.
6. Coordinate with clinical staff and ancillary departments to facilitate study procedures, such as laboratory tests, imaging studies, and specimen collection.
7. Assist with the preparation and submission of regulatory documents, institutional review board (IRB) submissions,



and other regulatory requirements as needed.
8. Participate in study-related meetings, training sessions, and conferences to stay abreast of relevant regulations, guidelines, and best practices in clinical research.
9. Maintain confidentiality of participant information and study data in accordance with applicable privacy laws and regulations.
10. Perform other duties as assigned by the principal investigator or research leadership team.
**Qualifications**:
1. Medical Doctor or relevant medical background
2. Prior experience working in a clinical research or healthcare setting strongly preferred.
3. Familiarity with Good Clinical Practice (GCP) guidelines, FDA regulations, and other applicable regulatory requirements governing clinical research.
4. Strong organizational skills with attention to detail and the ability to manage multiple tasks simultaneously.
5. Excellent communication skills, both written and verbal, with the ability to interact effectively with study participants, healthcare professionals, and research team members.
7. Ability to work independently and as part of a collaborative team environment.
8. Willingness to undergo training and certification as required by the institution or regulatory bodies.
Pay: From $358.00 per month
Ability to commute/relocate:
- Ciudad de México, CDMX: Reliably commute or planning to relocate before starting work (preferred)
**Language**:
- English / Spanish (preferred)
Work Location: In person

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📌 Pharmaceutical (Ciudad de México)
🏢 Clinical Trial Network
📍 Ciudad de México