Clinical Research Associate

**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 **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...

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...

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...

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...

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...

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...

Responsible for the management of clinical trials including investigator selection, analysis of potential patient recruitment, preparation of trial related documentation (Protocols, Case report forms, Investigators brochures, Consent documents, Letters of Agreement, Confidentiality Agreements), organizing trial related regulatory submissions with follow-up...

Responsible for the management of clinical trials including investigator selection, analysis of potential patient recruitment, preparation of trial related documentation (Protocols, Case report forms, Investigators brochures, Consent documents, Letters of Agreement, Confidentiality Agreements), organizing trial related regulatory submissions with follow-up...

Responsible for the management of clinical trials including investigator selection, analysis of potential patient recruitment, preparation of trial related documentation (Protocols, Case report forms, Investigators brochures, Consent documents, Letters of Agreement, Confidentiality Agreements), organizing trial related regulatory submissions with follow-up...

Responsible for the management of clinical trials including investigator selection, analysis of potential patient recruitment, preparation of trial related documentation (Protocols, Case report forms, Investigators brochures, Consent documents, Letters of Agreement, Confidentiality Agreements), organizing trial related regulatory submissions with follow-up...

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! The position will be based in Riyadh and reporting to the Clinical Operation Manager. **About the department** At the...

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....

Plans and manages patient-related research projects independently within a specifically defined field of study, but typically part of a clinical research program; analyses science-driven clinical studies; participates in writing papers and proposals; and supervises students and trainees. **Essential Responsibilities and Duties**: 2. Executes the results of...