Clinical Study Coordinator

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 experience....

**JOB TITLE**: **Clinical Study Administrator**: ***ABOUT ASTRAZENECA**: **AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading...

**JOB TITLE** **Clinical Study Administrator** **Location: Riyadh, KSA** **ABOUT ASTRAZENECA** AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the...

JOB TITLE:Clinical Study Administrator:ABOUT ASTRAZENECA:AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies.:ROLE...

**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...

**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...

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...

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...

Role PurposeThe 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 standards....

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...

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...

Assists and coordinates clinical research daily tasks required for research and/orclinical protocol; assists in a variety of complex activities involved in thecollection, compilation, documentation and analysis of clinical research dataunder the direction of a Principal Investigator or Project Leader. **Essential Responsibilities and Duties**: 1. Assists in...

**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...

**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...

The Position:Objectives and Scope of Position The Clinical Operations Hub Country Study Manager (CSM) provides leadership and hub strategic planning and operational delivery of assigned clinical studies through all phases of study management (preparation, study startup, conduct, closeout), in accordance with Roche quality standards, all applicable...

1. Oversees the daily schedule and operations of the clinic, supporting patient care for both the Dental Assisting and Dental Hygiene Programs, coordinates the assignment of patients, tracks and facilitates patient appointments.2. In collaboration with the Director, monitors and adjusts clinic practices to ensure compliance with MOH standards.3. Audits...

1. Oversees the daily schedule and operations of the clinic, supporting patient care for both the Dental Assisting and Dental Hygiene Programs, coordinates the assignment of patients, tracks and facilitates patient appointments.2. In collaboration with the Director, monitors and adjusts clinic practices to ensure compliance with MOH standards.3. Audits...

1. Oversees the daily schedule and operations of the clinic, supporting patient care for both the Dental Assisting and Dental Hygiene Programs, coordinates the assignment of patients, tracks and facilitates patient appointments.2. In collaboration with the Director, monitors and adjusts clinic practices to ensure compliance with MOH standards.3. Audits...

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...