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...

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...

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...

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...

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...

Contributes to the provision of safe, patient and family focused quality care. Provides comprehensive clinically focused staff orientation and professional development within area(s) of specialization utilizing the professional practice model. Supports the successful achievement of the Nursing Affairs (NA) strategic goals. **Essential Responsibilities and...

**Job Overview** Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. **Essential Functions** - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in...

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...

Responsible and accountable for the assessment, planning,implementation and evaluation of specialized care to a specific patientpopulation in collaboration with more senior clinical specialists and medicalstaff. **Essential Responsibilities and Duties**: - Obtains clinical histories, conducts physical examinations, and obtains tests related to area of...

Provides comprehensive clinically focused staff orientationand professional development within area(s) of specialization utilizing theprofessional practice model. **Essential Responsibilities and Duties**: Collaborates with the appropriate Education Coordinator(s) to ensure the educational needs of the assigned unit(s)/clinic(s) and/or group of nurses are...

**Job Overview** Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. **Essential Functions** - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in...

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 and accountablefor the assessment, planning, implementation, and evaluation of specializedcare to a specific patient population. Involves in research and staff educationand development. **Essential Responsibilities and Duties**: Obtains clinical histories, conducts physical examinations, and obtains tests related to area of specialisation....

Responsibilities; - Main Point of Contact (POC) for assigned protocols and link between Country Operations and Clinical Trial Team (CTT). - May support TA-Head / CRD with oversight of Therapeutic Area program(s) and strategy alignment as needed. - Responsible for project management of the assigned studies: pro-actively plans, drives and tracks execution and...