IQVIA

CRA 2 - HomebasedThis role is an ideal stepping-stone. Youll have training and development to plan and progress your career in the direction you choose. And you wont do it alone you will have dedicated mentoring and receive structured quarterly reviews on performance promotion and bo

CRA 2 - HomebasedThis role is an ideal stepping-stone. Youll have training and development to plan and progress your career in the direction you choose. And you wont do it alone you will have dedicated mentoring and receive structured quarterly reviews on performance promotion and bo

Internal Job DescriptionJob OverviewPerform a variety of clinical procedures to collect record report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol standard operating procedures (SOPs) and Good Clinical Practice (GCP).

Internal Job DescriptionJob OverviewPerform a variety of clinical procedures to collect record report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol standard operating procedures (SOPs) and Good Clinical Practice (GCP).

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly If so come and join us at IQVIA as - Clinical Trial Educator I Alzhe

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly If so come and join us at IQVIA as - Clinical Trial Educator I Alzhe

Key Responsibilities Serve as Regulatory Team Lead on complex global studies including oversight of technical writing and submission publishing. Draft review and quality-check clinical trial regulatory core study documentation at global and country level . Engage directly with clients

Key Responsibilities Serve as Regulatory Team Lead on complex global studies including oversight of technical writing and submission publishing. Draft review and quality-check clinical trial regulatory core study documentation at global and country level . Engage directly with clients

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly If so come and join us - IQVIA are looking Clinical Research Coordina

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly If so come and join us - IQVIA are looking Clinical Research Coordina

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.Essential Functions Oversee the execution

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.Essential Functions Oversee the execution

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly If so come and join us - IQVIA are looking Clinical Research Coordina

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly If so come and join us - IQVIA are looking Clinical Research Coordina

This Medical Advisor role will provide medical clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials.Serve as a medical expert during project delivery life-cycle. Provide therapeutic

This Medical Advisor role will provide medical clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials.Serve as a medical expert during project delivery life-cycle. Provide therapeutic

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 Functions Perform site monitoring visits (sele

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 Functions Perform site monitoring visits (sele

Job OverviewEngage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol standard operating procedures good clinical practice and applicable regulatory requirements.Essential Functions

Job OverviewEngage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol standard operating procedures good clinical practice and applicable regulatory requirements.Essential Functions

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 with contracted s

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 with contracted s

Job OverviewProvide project related assistance for assigned project(s) sites and project teams. Lead teams functionally where assigned including awareness of scope of work budget and resources. Ensure all work is conducted in accordance with SOPs policies and practices good clinical p

Job OverviewProvide project related assistance for assigned project(s) sites and project teams. Lead teams functionally where assigned including awareness of scope of work budget and resources. Ensure all work is conducted in accordance with SOPs policies and practices good clinical p

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 Functions Perform site monitoring visits (sele

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 Functions Perform site monitoring visits (sele

Clinical Trial Psych Rater - Czech SpeakingLocation: Remote/VirtualHours: Estimated 1016 hours per monthRole: Clinical SpecialistAbout IQVIAIQVIA is a global leader in advanced analytics technology solutions and clinical research services dedicated to driving healthcare forward. We pa

Clinical Trial Psych Rater - Czech SpeakingLocation: Remote/VirtualHours: Estimated 1016 hours per monthRole: Clinical SpecialistAbout IQVIAIQVIA is a global leader in advanced analytics technology solutions and clinical research services dedicated to driving healthcare forward. We pa

Location: Mexico Argentina or Brazil (Remote must be available to work Eastern or Central U.S. time zones)100% home based roleWe are seeking an experienced Principal Statistician to join our BIOS team for one of our FSP clients. This advanced-level position requires strong expertise

Location: Mexico Argentina or Brazil (Remote must be available to work Eastern or Central U.S. time zones)100% home based roleWe are seeking an experienced Principal Statistician to join our BIOS team for one of our FSP clients. This advanced-level position requires strong expertise

To provide comprehensive administrative support to the field based staff of a single large project or multiple projects.Essential Functions To work collaboratively across the Team Coordinator function and understand how the function contributes to the Commercial business. To be the fi

To provide comprehensive administrative support to the field based staff of a single large project or multiple projects.Essential Functions To work collaboratively across the Team Coordinator function and understand how the function contributes to the Commercial business. To be the fi

Our MedTech Technical Support Representative opportunity would see you supporting a leading medical device manufacturers software update needs on equipment based in hospitals pharmacies and other clinical settings. The current product line being supported is an automated medication di

Our MedTech Technical Support Representative opportunity would see you supporting a leading medical device manufacturers software update needs on equipment based in hospitals pharmacies and other clinical settings. The current product line being supported is an automated medication di

Sales RepresentativeAbout the Role:We are seeking a motivated and results-driven Pharmaceutical Sales Representative to join our this role you will be responsible for driving volume and market share growth for assigned pharmaceutical products within a designated territory. You will b

Sales RepresentativeAbout the Role:We are seeking a motivated and results-driven Pharmaceutical Sales Representative to join our this role you will be responsible for driving volume and market share growth for assigned pharmaceutical products within a designated territory. You will b

Trainer Patient Support Services (Per Diem)This per diem Trainer role is aligned with IQVIAs Centralized Outsourcing Operations Hub (COOH) team supporting Patient Support Services in a call center this project-based per diem Trainer role for Patient Support Services you will be prima

Trainer Patient Support Services (Per Diem)This per diem Trainer role is aligned with IQVIAs Centralized Outsourcing Operations Hub (COOH) team supporting Patient Support Services in a call center this project-based per diem Trainer role for Patient Support Services you will be prima

Join IQVIAs Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes.In this role youll work closely wit

Join IQVIAs Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes.In this role youll work closely wit