Clinical Research Coordinator

Participates in designing and executing clinical research tasks required for research and/or clinical protocols; coordinates and participates in various complex activities involved in collecting, compiling, documenting, and analyzing clinical research data under the direction of a Principal Investigator or Project Leader. **Essential Responsibilities and...

Participates in designing and executing clinical research tasksrequired for research and/or clinical protocols; coordinates and participatesin a variety of complex activities involved in the collection, compilation,documentation and analysis of clinical research data under the direction of aPrincipal Investigator or Project Leader. **Essential...

Role Purpose The Clinical Research Coordinator (“CRC”) comprises an integral part of the research team at the Sites level. Working in coordination with the Principal Investigator, he/she is responsible to support the Principal Investigator in conducting the Study in accordance with ICH-GCP, regulatory standards, Protocol study design and client...

Responsible for increasing the quality and quantity ofclinical research performed in the Department and therefore promote anatmosphere of serious enquiry among all members of the department especially thejunior staff. **Essential Responsibilities and Duties**: 1. Maintains an updated log book of all approved clinical research protocols stating the dates of...

**Clinical Research Manager / FSP Manager** **Job Purpose/Summary** Responsible for staffing and managing Employee, Consultant or Freelance CTA, Clinical Research Associates (CRAs), Clinical Monitoring Associates (CMAs), or In-House Clinical Research Associates (ICRAs) and ensuring adherence to and implementation of CTI policies. Manage quality and...

**Clinical Research Associate (level dependent on experience)** **Job Purpose/Summary** As a CRA you will be responsible for the successful conduct of clinical trials and serve as the main contact for the investigative site by representing CTI in a professional manner. **What You’ll Do** - Conduct evaluation, initiation, monitoring and close out...

Join **RAY CRO** as a Clinical Study Coordinator! We're seeking motivated individuals in Riyadh to contribute to advancing medical research. As a Coordinator, you'll oversee study activities, collaborate with investigators, and ensure protocol adherence. **Qualifications**: - Bachelor's degree in a relevant field. - Previous clinical study coordination...

Supervises and provides leadership to medical technology service teams, within the Clinical Engineering Department, that provide for the operational and technical support od medical diagnostic, therapeutic and analytical devices and systems, utilized for applied patient healthcare and healthcare research. Acts as the senior operational and technical resource...

Coordinates comprehensivestaff professional development within area of specialization to supportevidence based delivery system that produces quality patient care with optimalpatient outcomes. **Essential Responsibilities and Duties**: Evaluates and initiates plans for nursing research into practice in line with overall Nursing Affairs (NA) strategies.-...

Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, with or without guidance, liaise with vendors; and other duties, as assigned - Responsible for aspects of registry management as prescribed in the project plans - General...