Clinical Research Coordinator

hace 2 semanas

Tláhuac, Ciudad de México Clinical Trial Network A tiempo completo

Job Title:
Clinical Research Coordinator

Location:
Houston, Texas

Company:
Clinical Trial Network

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:

  • Coordinate and manage all aspects of clinical research studies, including participant recruitment, enrollment, and follow-up.
  • Ensure compliance with regulatory requirements, including obtaining informed consent, adherence to study protocols, and maintaining accurate and complete study documentation.
  • Collaborate with principal investigators, study sponsors, and other stakeholders to develop study protocols and research objectives.
  • Schedule and conduct study visits, collect and process study-related data, and ensure timely and accurate data entry into study databases.
  • Monitor participant safety and adverse events throughout the course of the study, and report any concerns or deviations from protocol to the appropriate parties.
  • Coordinate with clinical staff and ancillary departments to facilitate study procedures, such as laboratory tests, imaging studies, and specimen collection.
  • Assist with the preparation and submission of regulatory documents, institutional review board (IRB) submissions, and other regulatory requirements as needed.
  • Participate in study-related meetings, training sessions, and conferences to stay abreast of relevant regulations, guidelines, and best practices in clinical research.
  • Maintain confidentiality of participant information and study data in accordance with applicable privacy laws and regulations.
  • Perform other duties as assigned by the principal investigator or research leadership team.

Qualifications:

  • Medical Doctor or relevant medical background
  • Prior experience working in clinical research or healthcare setting strongly preferred.
  • Familiarity with Good Clinical Practice (GCP) guidelines, FDA regulations, and other applicable regulatory requirements governing clinical research.
  • Strong organizational skills with attention to detail and the ability to manage multiple tasks simultaneously.
  • Excellent communication skills, both written and verbal, with the ability to interact effectively with study participants, healthcare professionals, and research team members.
  • Ability to work independently and as part of a collaborative team environment.
  • Willingness to undergo training and certification as required by the institution or regulatory bodies.

Pay:
$ $25.00 per hour

Expected hours: 40 per week

Ability to Relocate:

  • Ciudad de México: Relocate before starting work (required)

Work Location:
In person

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