Career Opportunities at a Clinical Research Center
Triple O Research Institute is offering several different career opportunities at our clinical research center. You can do your part in helping us provide better healthcare to people all around the world. We are currently recruiting for the following positions:
* Study Coordinators:
As a Study Coordinator, you will be responsible for managing the day-to-day operations of clinical trials and research studies. Your duties will include recruiting and enrolling participants, collecting and processing patient’s samples, ensuring compliance with regulatory standards, coordinating with other research staff, and maintaining accurate study documentation.
(This is a full-time, on-site position.)
* Medical Assistants:
As a Medical Assistant, you will be responsible for supporting study coordinator, healthcare providers in delivering patient care. Your duties will include taking patient histories, recording vital signs, assisting with medical examinations, collecting and processing blood and urine samples, managing patient records, and scheduling appointments.
(This is a full-time, on-site position.)
* Regulatory Contract Specialists:
As a Regulatory Contract Specialist, you will be responsible for managing and updating regulatory documents, contracts related to clinical research and trials. Your duties include drafting, reviewing, and updating IRB forms such as ICF, contract terms, ensuring compliance with legal and regulatory requirements, and liaising with internal and external stakeholders to facilitate contract execution and adherence.
(This is a full-time, on-site position.)
* Data Entry Personnel:
As Data Entry Personnel, you will be responsible for accurately entering and updating data into various electronic systems. Your duties will include verifying and correcting data, maintaining detailed records, and ensuring that information is entered promptly and accurately for project needs.
(This is a full-time, on-site position.)
