IQVIA

Our Field Service Technicians experience a unique opportunity to employ their technical experience by collaborating with healthcare professionals and leading technical initiatives in medical device technology. You will be responsible for troubleshooting repairing and updating medical

Our Field Service Technicians experience a unique opportunity to employ their technical experience by collaborating with healthcare professionals and leading technical initiatives in medical device technology. You will be responsible for troubleshooting repairing and updating medical

Job overview:The Adverse Event Intake Coordinator plays a critical role in ensuring the timely and accurate processing of adverse event reports related to our companys products. This position is responsible for receiving reviewing and processing incoming adverse event reports (AEs) fr

Job overview:The Adverse Event Intake Coordinator plays a critical role in ensuring the timely and accurate processing of adverse event reports related to our companys products. This position is responsible for receiving reviewing and processing incoming adverse event reports (AEs) fr

The Associate Decentralized Clinical Trial Study Lead (aDCTL) / Decentralized Clinical Trial Lead (DCTL) are an integral part of clinical trial delivery to improve patients lives and bring therapies to the market faster. The aDCTL / DCTL roles requires strong project management skills

The Associate Decentralized Clinical Trial Study Lead (aDCTL) / Decentralized Clinical Trial Lead (DCTL) are an integral part of clinical trial delivery to improve patients lives and bring therapies to the market faster. The aDCTL / DCTL roles requires strong project management skills

Job Description SummaryAn excellent opportunity for students eager to launch their Clinical Research careers while gaining practical experience in Clinical Trial Agreement support Contract Negotiation processes and Country Site Activation activities.Key ResponsibilitiesThe intern will

Job Description SummaryAn excellent opportunity for students eager to launch their Clinical Research careers while gaining practical experience in Clinical Trial Agreement support Contract Negotiation processes and Country Site Activation activities.Key ResponsibilitiesThe intern will

Clinical Trials Regulatory OfficerJob SummaryThe Clinical Trials Regulatory Officer prepares reviews and manages regulatory documentation to support clinical trial submissions in compliance with applicable regulatory requirements. The role provides regulatory support across clinical t

Clinical Trials Regulatory OfficerJob SummaryThe Clinical Trials Regulatory Officer prepares reviews and manages regulatory documentation to support clinical trial submissions in compliance with applicable regulatory requirements. The role provides regulatory support across clinical t

This is an exciting opportunity to work as an Associate Consultant in IQVIA one of the worlds leading multi-disciplinary and cross-functional teams working with Real World patient data to help our client base answer their key business questions make more informed decisions and deliver

This is an exciting opportunity to work as an Associate Consultant in IQVIA one of the worlds leading multi-disciplinary and cross-functional teams working with Real World patient data to help our client base answer their key business questions make more informed decisions and deliver

Clinical Lead (Clinical Trial Management) - Global Study LeadershipAt IQVIA our Clinical Leads play a vital role in bringing innovative medicines to patients worldwide. Youll provide clinical leadership across regional and global clinical trials partnering with Project Leaders sponsor

Clinical Lead (Clinical Trial Management) - Global Study LeadershipAt IQVIA our Clinical Leads play a vital role in bringing innovative medicines to patients worldwide. Youll provide clinical leadership across regional and global clinical trials partnering with Project Leaders sponsor

PURPOSEThe Internal Translator is responsible for linguistically and culturally interpreting the written material in a way that maintains or duplicates the structure and style of the original text while keeping the ideas and facts of the original material accurate.They possess fluency

PURPOSEThe Internal Translator is responsible for linguistically and culturally interpreting the written material in a way that maintains or duplicates the structure and style of the original text while keeping the ideas and facts of the original material accurate.They possess fluency

This is an exciting opportunity to work as an Associate Consultant in IQVIA one of the worlds leading multi-disciplinary and cross-functional teams working with Real World patient data to help our client base answer their key business questions make more informed decisions and deliver

This is an exciting opportunity to work as an Associate Consultant in IQVIA one of the worlds leading multi-disciplinary and cross-functional teams working with Real World patient data to help our client base answer their key business questions make more informed decisions and deliver

Clinical Lead (Clinical Trial Management) - Global Study LeadershipAt IQVIA our Clinical Leads play a vital role in bringing innovative medicines to patients worldwide. Youll provide clinical leadership across regional and global clinical trials partnering with Project Leaders sponsor

Clinical Lead (Clinical Trial Management) - Global Study LeadershipAt IQVIA our Clinical Leads play a vital role in bringing innovative medicines to patients worldwide. Youll provide clinical leadership across regional and global clinical trials partnering with Project Leaders sponsor

PURPOSEThe Internal Translator is responsible for linguistically and culturally interpreting the written material in a way that maintains or duplicates the structure and style of the original text while keeping the ideas and facts of the original material accurate.They possess fluency

PURPOSEThe Internal Translator is responsible for linguistically and culturally interpreting the written material in a way that maintains or duplicates the structure and style of the original text while keeping the ideas and facts of the original material accurate.They possess fluency

The Associate Decentralized Clinical Trial Study Lead (aDCTL) / Decentralized Clinical Trial Lead (DCTL) are an integral part of clinical trial delivery to improve patients lives and bring therapies to the market faster. The aDCTL / DCTL roles requires strong project management skills

The Associate Decentralized Clinical Trial Study Lead (aDCTL) / Decentralized Clinical Trial Lead (DCTL) are an integral part of clinical trial delivery to improve patients lives and bring therapies to the market faster. The aDCTL / DCTL roles requires strong project management skills

Job Description SummaryAn excellent opportunity for students eager to launch their Clinical Research careers while gaining practical experience in Clinical Trial Agreement support Contract Negotiation processes and Country Site Activation activities.Key ResponsibilitiesThe intern will

Job Description SummaryAn excellent opportunity for students eager to launch their Clinical Research careers while gaining practical experience in Clinical Trial Agreement support Contract Negotiation processes and Country Site Activation activities.Key ResponsibilitiesThe intern will

Clinical Trials Regulatory OfficerJob SummaryThe Clinical Trials Regulatory Officer prepares reviews and manages regulatory documentation to support clinical trial submissions in compliance with applicable regulatory requirements. The role provides regulatory support across clinical t

Clinical Trials Regulatory OfficerJob SummaryThe Clinical Trials Regulatory Officer prepares reviews and manages regulatory documentation to support clinical trial submissions in compliance with applicable regulatory requirements. The role provides regulatory support across clinical t

Job overview:The Adverse Event Intake Coordinator plays a critical role in ensuring the timely and accurate processing of adverse event reports related to our companys products. This position is responsible for receiving reviewing and processing incoming adverse event reports (AEs) fr

Job overview:The Adverse Event Intake Coordinator plays a critical role in ensuring the timely and accurate processing of adverse event reports related to our companys products. This position is responsible for receiving reviewing and processing incoming adverse event reports (AEs) fr

Project Leads are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to mee

Project Leads are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to mee

Job OverviewProvides information technology support across a range of products and platforms.Works closely with the OneKey (healthcare professional Database) operation team to manage and align processes.Maintains continuous communication with clients to understand their requests and i

Job OverviewProvides information technology support across a range of products and platforms.Works closely with the OneKey (healthcare professional Database) operation team to manage and align processes.Maintains continuous communication with clients to understand their requests and i

Job DescriptionMake real impact by helping patients adopt healthier habits manage chronic conditions and navigate this field-based role youll deliver primarily face-to-face wellness coaching coordinate care and educate patients on treatment plans and devices. Youll ensure timely foll

Job DescriptionMake real impact by helping patients adopt healthier habits manage chronic conditions and navigate this field-based role youll deliver primarily face-to-face wellness coaching coordinate care and educate patients on treatment plans and devices. Youll ensure timely foll

Clinical Independent Rater (CIR) Japanese SpeakingStudy: M26-298Location: Remote/VirtualHours: Estimated 1016 hours per monthRole: Clinical Independent Rater (CIR)About IQVIAIQVIA is a global leader in advanced analytics technology solutions and clinical research services dedicated t

Clinical Independent Rater (CIR) Japanese SpeakingStudy: M26-298Location: Remote/VirtualHours: Estimated 1016 hours per monthRole: Clinical Independent Rater (CIR)About IQVIAIQVIA is a global leader in advanced analytics technology solutions and clinical research services dedicated t

Role OverviewThe Global Asset/Commercialization Partner is a senior client leadership role responsible for helping Emerging Biopharma companies successfully navigate the journey from asset development to commercialization and lifecycle growth. Acting as a trusted advisor to executive

Role OverviewThe Global Asset/Commercialization Partner is a senior client leadership role responsible for helping Emerging Biopharma companies successfully navigate the journey from asset development to commercialization and lifecycle growth. Acting as a trusted advisor to executive