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IQVIA in Riyadh, Saudi Arabia seeks an on-site Clinical Research Monitor to ensure sites conduct studies per protocol, applicable regulations and sponsor requirements. Responsibilities include performing site monitoring visits (selection, initiation, monitoring and close-out), supporting subject recruitment, administering training, maintaining TMF/ISF, 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...

Work ScheduleEnvironmental ConditionsJob DescriptionJoin Us as a Clinical Research Associate (Level II) IVD and Clinical Make an Impact at the Forefront of Innovation.We 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 team...

Job Description SummaryThe SSO Study StartUp Manager is accountable for study planning SSU activities and activation deliverables of assigned projects in compliance with Novartis processes GCP/ICH and regulatory requirements in a standalone country OPC (operating country) or satellite country. Leads all SSU activities of assigned projects in close...

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 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 research and support scientific advancements in an ambitious and collaborative...

CTI Clinical Trial and Consulting Services in Riyadh, Saudi Arabia, seeks a Clinical Research Associate to support successful conduct of trials and act as the main site contact for CTI.Responsibilities include performing initiation, monitoring and close-out visits, supporting regulatory start-up activities, ensuring data integrity and timelines, and...

The Local Clinical Project Manager(Sponsor dedicated) will be leading Local Study Teams at country level to deliver committed components of clinical studies according to agreed resources budget and timelines complying with Sponsor Procedural Documents international guidelines such as ICH-GCP as well as relevant local regulations.In addition to leading the...

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner and safer. We provide our colleagues with the...

IQVIA is seeking a Local Clinical Project Manager in Riyadh to lead country-level study teams and deliver clinical trial components on time and within budget, while complying with ICH-GCP and local regulations.The role may include site monitoring, site qualification, regulatory submissions, budget management, CTMS setup, and ensuring essential documents are...

About This Role As an Associate Clinical Country & Site Lead you will be in an external-facing country-aligned clinical operations position focused on providing key local operational and scientific knowledge to support country-level clinical development strategy. You will help enable local partnerships enhance customer satisfaction and support the focused...

IQVIA, Inc. is seeking a Local Clinical Project Manager to lead country-level study teams in Saudi Arabia, ensuring on-time delivery of high-quality data in accordance with Sponsor procedures and ICH-GCP.The role may include site monitoring to support capacity and local regulatory activities. You will coordinate site selection, feasibility assessments,...

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...

CTI Clinical Trial and Consulting Services is seeking a capable clinical trial monitor in Saudi Arabia to oversee monitoring activities from Phase I to IV and Real World Evidence studies. You will develop knowledge of drug development, ICH GCP, and regulatory guidelines while managing study site activities in line with SOPs.Responsibilities include...

The Local Clinical Project Manager (Sponsor dedicated) will be leading Local Study Teams at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Sponsor Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations.In addition to leading the...

Job OverviewPerform 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 FunctionsPerform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with...

Job Overview: Local Clinical Project Management services provides local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries. Services/deliverables include operational oversight of assigned protocol(s) at the country level from start-up through to database lock and closeout activities. Further services will...

Job OverviewDirect a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives. Work with senior leadership in formulating effective strategic goals and objectives for designated organization and assures operational alignment with organization...

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...

Job OverviewDirect and manage the delivery of all required site activation maintenance and regulatory activities for selected studies or multi-protocol programs including pre-award activities oversight of the scope of work budget and resources.This role requires a candidate strong in regulatory experience with finance experience as a benefit. Arabic language...