cra

About the job Responsible for project activities associated with monitoring functions of phase I through phase IV clinical research studies and Real World Evidence (RWE) studies, while continuing to develop knowledge of drug development process, International Council for Harmonisation (ICH) / Good Clinical Practice (GCP), and relevant regulations.  Performs...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Research Associate – Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.As part of our global...

Job OverviewThe Study StartUp CRA is accountable for site selections as well as studyspecific startup activities and deliverables of assigned sites for Phase IIV trials in the country in accordance with monitoring procedures and processes following ICH/GCP local regulations and SOPs. Proactive site preparation and early identification of real site needs and...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Research Associate (Level II) Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 countries in the last 5 years.As part of our global...

Education and Experience Requirements: Bachelor's degree in Microbiology or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification. Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2 years as a clinical research monitor) or completion of PPD Drug...

About The Job Responsible for project activities associated with monitoring functions of phase I through phase IV clinical research studies and Real World Evidence (RWE) studies, while continuing to develop knowledge of drug development process, International Council for Harmonisation (ICH) / Good Clinical Practice (GCP), and relevant regulations. Performs...

Responsible for project activities associated with monitoring functions of Phase I through Phase IV clinical research studies and Real World Evidence (RWE) studies, while continuing to develop knowledge of drug development process, International Council for Harmonisation (ICH) / Good Clinical Practice (GCP), and relevant regulations. Performs management of...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office Join Us as a Clinical Research Associate - Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. **What You’ll...

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsFluctuating Temps hot/cold Office Various outside weather conditionsJob DescriptionAbout the RoleJoin Thermo Fisher Scientific Inc. as a Sr. Clinical Research Associate based in Saudi Arabia and be part of an outstanding team! This is an outstanding opportunity to contribute to groundbreaking...

IQVIA Saudi Arabia is looking for talented and motivated team member to join our Multi-Sponsored team as junior CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.Under...

About the job Responsible for project activities associated with monitoring functions of Phase I through Phase IV clinical research studies and Real World Evidence (RWE) studies, while continuing to develop knowledge of drug development process, International Council for Harmonisation (ICH) /  Good Clinical Practice (GCP), and relevant regulations. ...

About The Job Responsible for project activities associated with monitoring functions of phase I through phase IV clinical research studies and Real World Evidence (RWE) studies, while continuing to develop knowledge of drug development process, International Council for Harmonisation (ICH) / Good Clinical Practice (GCP), and relevant regulations. Performs...

Associate Clinical Research AssociateIQVIA is looking for talented and motivated team member to join our Multi-Sponsored team as junior CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our...

**About the job** Responsible for project activities associated with monitoring functions of phase I through phase IV clinical research studies and Real World Evidence (RWE) studies, while continuing to develop knowledge of drug development process, International Council for Harmonisation (ICH) / Good Clinical Practice (GCP), and relevant regulations....

Job OverviewPerform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

Job OverviewPerform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

IQVIA is seeking a Clinical Research Associate (CRA) to advance your career with dedicated mentoring and structured performance reviews. The role focuses on site selection, initiation, monitoring, and close-out visits, alongside developing recruitment plans and ensuring protocol training across sites.Ideal candidates have 1.5–2 years of on-site monitoring...

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential Functions• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

Risk Manager – Hospitality Construction Projects (Mega & Giga Projects) Role Purpose Lead and manage the project risk management function for large-scale hospitality developments, ensuring proactive identification, assessment, mitigation, monitoring, and reporting of risks across design, procurement, construction, commissioning, and handover phases. The...

We are seeking a Piping Materials Metallurgy SME to serve as the Technical Authority across our portfolio of energy oil amp gas mining industrial and infrastructure projects in Saudi Arabia The successful candidate will provide technical leadership throughout the project lifecycle including proposals concept studies FEED detailed engineering construction...