clinical study

TFS HealthScience in the United Arab Emirates is a leading global mid-size CRO, partnering with biopharma across the full clinical development journey. The Project Director will lead the operational planning, execution and oversight of global studies, including observational and interventional designs, while ensuring delivery within time, budget and...

TFS HealthScience in the United Arab Emirates is a leading global mid-size CRO, partnering with biopharma across the full clinical development journey. The Project Director will lead the operational planning, execution and oversight of global studies, including observational and interventional designs, while ensuring delivery within time, budget and...

TFS HealthScience in the United Arab Emirates is a leading global mid-size CRO, partnering with biopharma across the full clinical development journey. The Project Director will lead the operational planning, execution and oversight of global studies, including observational and interventional designs, while ensuring delivery within time, budget and quality....

Dubai, United Arab Emirates | Posted on 09/03/2025 We are seeking a highly skilled and experienced Clinical Neuro Psychologist to join one of our reputed hospitals in Dubai. This roleis ideal for professionals who have completed their clinical training and arelooking to advance their career in neuro-psychological research, specializedclinical practice, or...

Dubai, United Arab Emirates | Posted on 09/03/2025 We are seeking a highly skilled and experienced Clinical Neuro Psychologist to join one of our reputed hospitals in Dubai. This roleis ideal for professionals who have completed their clinical training and arelooking to advance their career in neuro-psychological research, specializedclinical practice, or...

ResponsibilitiesLead all clinical study operations including strategic/tactical planning, timelines, budgets, and site management Facilitate communication between sponsors, study teams, and functional groups Manage and mentor study team members to ensure professional development Provide financial oversight of study budgets and track out-of-scope...

Responsibilities - Lead all clinical study operations including strategic/tactical planning, timelines, budgets, and site management - Facilitate communication between sponsors, study teams, and functional groups - Manage and mentor study team members to ensure professional development - Provide financial oversight of study budgets and track out-of-scope...

**JOB PURPOSE**: The CRA will be responsible for clinical site management including monitoring to fully ensure patient safety, verification of source data versus Case Report Forms (CRFs) to ensure accuracy and completeness of data in compliance with protocol (s), Federal regulations, ICH & GCPs. Helps to ensure that the quality of work and data are suitable...

About the jobThis position is 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...

About the jobThis position is 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...

About the jobThis position is 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...

About the jobThis position is 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...

About the jobThis position is 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...

About the jobThis position is 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...

About the jobThis position is 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...

Clinical Ink is seeking an eSource Developer III to join our Study Operations team, working remotely across the United States. You will design and build electronic source documents aligned with protocol requirements, ensuring quality, consistency, and usability while mentoring other team members.This role partners with cross-functional stakeholders, applies...

Clinical Ink is seeking an eSource Developer III to join our Study Operations team, working remotely across the United States. You will design and build electronic source documents aligned with protocol requirements, ensuring quality, consistency, and usability while mentoring other team members.This role partners with cross-functional stakeholders, applies...

Clinical Ink is seeking an eSource Developer III to join our Study Operations team, working remotely across the United States. You will design and build electronic source documents aligned with protocol requirements, ensuring quality, consistency, and usability while mentoring other team members.This role partners with cross-functional stakeholders, applies...

Clinical Ink is seeking an eSource Developer III to join our Study Operations team, working remotely across the United States. You will design and build electronic source documents aligned with protocol requirements, ensuring quality, consistency, and usability while mentoring other team members.This role partners with cross-functional stakeholders, applies...

Clinical Ink is seeking an eSource Developer III to join our Study Operations team, working remotely across the United States. You will design and build electronic source documents aligned with protocol requirements, ensuring quality, consistency, and usability while mentoring other team members.This role partners with cross-functional stakeholders, applies...