Assistant 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...

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...

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....

**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...

**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...

Coordinating various administrative functions and providing support to the Section. Assists in ensuring compliance with national and international research regulations, ethical standards, and Hospital’s policies. **Essential Responsibilities and Duties**: 1. Assists in obtaining necessary approvals from national and international research regulatory...

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...

Provides functional and logístical assistance to support clinical departments’ daily operations. **Essential Responsibilities and Duties**: - Participates in Patient reception duties. - Assists patients in understanding instructions from health care providers. - Assists in translating Arabic/English information for health providers and healthcare...

Responsible for non-physician clinical operations and patient care. Works closely with the Director, Organ Transplant Centre (OTC) to maintain and advance the safety, quality, compliance and professional competence of those who provide care to the transplant patient including all nursing, clinical and support services staff. Supervises transplant clinical...

Responsible for non-physician clinical operations and patient care. Works closely with the Director, Organ Transplant Centre (OTC) to maintain and advance the safety, quality, compliance and professional competence of those who provide care to the transplant patient including all nursing, clinical and support services staff. Supervises transplant clinical...

In Novo Nordisk Saudi Arabia, the position of Clinical Research Associate (CRA) provides you the opportunity to work in a high-performing team to contribute directly towards the business results while creating value for patients. The position will be based in Riyadh, Saudi Arabia, and report to the Clinical Operation Manager. **The Position** Being the...

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...

Clinical Research Associate **Category**:Clinical Development**Location**:Riyadh, Riyadh, SA- Are you a dedicated clinical trial professional with direct site management experience? Are you highly motivated by being able to make a difference in improving patients’ lives? If yes, keep reading - this role might be just for you!- Novo Nordisk is on the...

Responsible for non-physician clinical operations and patient care. Works closely with the Director, Organ Transplant Centre (OTC) to maintain and advance the safety, quality, compliance and professional competence of those who provide care to the transplant patient including all nursing, clinical and support services staff. Supervises transplant clinical...