Location: Remote, candidates must be based in the US Join IQVIA’s 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 outco......
Hiring In Durham, North Carolina, United States of Ame......
full-time Sourced
OND GeneralIQVIA Hol...ScraperLoicx
Job Overview Perform 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 (selection, in......
CRA - Czech Republic - One Sponsor- Homebased Would you like to be one of us? Are you eager to change and achieve new steps in your professional career? IQVIA is looking for a Clinical Research Associate to provide service to one of our sponsors. You would be responsible for: Performing visits (suc......
Job Overview Perform 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 (selection, i......
Experienced Clinical Research Associate, Italy Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance with regulatory requ......
Job Overview Clinical Research Associate performs monitoring and site management work to ensure that sites are conducting the studies and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions: • Perform site moni......
Job Overview Perform 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 (selection, in......
Hiring In Parsippany, New Jersey, United States of Ame......
Job Overview: Perform 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 (selection......
Hiring In Durham, North Carolina, United States of Ame......
Clinical Research Associate IQVIA Turkey is looking for talented and motivated team member to join our Sponsor dedicated 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 thera......
Senior Clinical Research Associate IQVIA is the Human Data Science Company oriented to drive human health outcomes forward. When you join IQVIA Turkey as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct expe......
Clinical Research Associate IQVIA Bucharest is looking for talented and motivated team member to join our Sponsor dedicated 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 the......
IQVIA is hiring Clinical Research Associates (CRA) at the 1 and 2 level. Ideal candidates will have 1-2 years of onsite monitoring experience with expertise in Cardiovascular/Renal/Metabolic, Oncology, and/or Neurology. Candidates can be located anywhere in the US. Job Overview Perform monitoring an......
Hiring In Overland Park, KS, United States of America
Clinical Trial Manager – Sponsor Dedicated. Clinical Project Management services provide management of a clinical trial (s) in a local level. Services/deliverables include operational oversight of assigned project(s) at country level for end-to-end project management from start-up through to closeou......
Associate Site Activation Manager – Sponsor Dedicated Direct 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 and resources. You will: Overse......
Join Us on Our Mission to Drive Healthcare Forward IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. Why IQVIA? IQVIA is recognized as #1 in its category on the 2025 Fortune® World’s Most Admired Companies™ list for the FOURTH consecutive year! We offer g......
Join Us on Our Mission to Drive Healthcare Forward IQVIA cFSP (sponsor-dedicated) are seeking experienced Senior Clinical Research Associates in the UK. Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by......
Clinical Research Associate IQVIA Bucharest is looking for talented and motivated team member to join our Sponsor dedicated 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 the......
Job Overview Join our team as a Clinical Research Site Manager, where you’ll play a crucial role in ensuring our study sites operate seamlessly and adhere to all protocols, regulations, and sponsor requirements. Essential Functions Site Monitoring: Conduct selection, initiation, monitoring, and cl......
To be eligible for this position, you must reside in the same country where the job is located. Seeking experienced candidates near major hub airports in the Southeast, Northeast, Central and West regions. Job Overview Perform monitoring and site management work to ensure that sites are conducti......
Hiring In Durham, North Carolina, United States of Ame......
To be eligible for this position, you must reside in the same country where the job is located. Perform 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 sponso......
Hiring In Durham, North Carolina, United States of Ame......
Clinical Research Associate Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Go......
We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available. As Clinical Trial Assistant, you will be working in our Clinical Trials Team together with some of the most talented people in the field and gain a brought knowled......
IQVIA is hiring Clinical Research Associates! Join IQVIA today and make an impact on patients’ outcome! Job Overview Perform 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 g......
Join Us on Our Mission to Drive Healthcare Forward IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the st......
Job Overview Collaborate with pre and post award stakeholders to manage the coordination, planning, quality and implementation of Patient Recruitment and Retention operational plans on small/mid size studies. Position may be responsible for the implementation of smaller programs in their entirety. C......
Job Overview As you develop your career as a CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA™, we do not believe in a ‘career ceiling.’ You can make the Senior CRA role a stepping-stone into wider opportunities like operations manageme......
Job Overview 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......
Hiring In Lisbon, Portugal
full-time Sourced
OND 5-yearsIQVIA Hol...ScraperLoicx
Job Overview Manage 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. Essential Functions • Manage staff in accordance with organization’s policies and applicable regulations. Respo......
Hiring In Seoul, Republic of Korea
full-time Sourced
OND 1-yearsIQVIA Hol...ScraperLoicx
Job Overview : Responsible for managing the end-to-end contract paperwork process. Responsible for contract process quality control and sending executed contracts and amendments as appropriate to third parties. Perform data entry and pull reports from tracking database(s). Contact third parties t......
Hiring In Paris, France
full-time Sourced
OND 3-yearsIQVIA Hol...ScraperLoicx
Join IQVIA’s 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, you’ll work closely with one spons......
Hiring In Durham, North Carolina, United States of Ame......
full-time Sourced
OND GeneralIQVIA Hol...ScraperLoicx
Internal Job Description Clinical Trial Manager – Sponsor Dedicated. Clinical Project Management services provide management of a clinical trial (s) in a regional level. Services/deliverables include operational oversight of assigned project(s) at the regional level for end-to-end project management......
This role follows a hybrid model and requires working 2–3 days per week from the sponsor’s offices. Job Overview 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 e......
Hiring In Copenhagen, Denmark
full-time Sourced
OND 5-yearsIQVIA Hol...ScraperLoicx
About the job: Local Trial 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 loc......
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to manage Early Phase clinical research projects in different therapeutic areas and ......
Hiring In Frankfurt, Hesse, Germany
full-time Sourced
OND 2-yearsIQVIA Hol...ScraperLoicx
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to work with one single client and to manage clinical research projects in different......
Hiring In Athens, Greece
full-time Sourced
OND 5-yearsIQVIA Hol...ScraperLoicx
Global Trial Delivery Manager services provide for the global coordination of clinical trial management activities for internally managed and/or outsourced trials. These services lead the Study Management Team (SMT) and ensure global clinical operations deliverables progress according to agreed upon......
Job Overview Perform 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 (selection, in......
Hiring In Overland Park, KS, United States of America
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to work with one single client and to manage clinical research projects in different t......
Hiring In Vienna, Austria
full-time Sourced
OND 5-yearsIQVIA Hol...ScraperLoicx
The Senior Clinical Operations Lead will be responsible to support the Clinical Trial Manager/operational team in execution of the trial(s). The function could include direct liaison with CROs and other ancillary vendors, as appropriate, to manage relevant trial(s) operational tasks. Maintain effect......
Vue d’ensemble du poste Effectuer des tâches de suivi et de gestion de site pour une variété de protocoles, de sites et de domaines thérapeutiques. Doit être bilingue français et anglais et situé à Montréal. Responsabilités essentielles • Effectuer des visites de suivi des sites (visites de s......
Vue d’ensemble du poste Effectuer des tâches de suivi et de gestion de site pour une variété de protocoles, de sites et de domaines thérapeutiques. Doit être bilingue français et anglais et situé à Montréal. Responsabilités essentielles • Effectuer des visites de suivi des sites (visites de s......
The Study Start-Up (SSU) Lead plans and executes global SSU activities to ensure timely trial document and task completion to enable country HA (Health Authorities) and Ethics Committee submissions and site activation to meet ambitious recruitment plans. The Study Start-Up Lead works collaboratively......
Hiring In Bratislava, Slovakia
full-time Sourced
OND 6-yearsIQVIA Hol...ScraperLoicx
Job Purpose Location: home-based, Slovakia & Romania The Associate Director Senior Study Lead is the leader of the cross-functional clinical trial team (CTT), who guides planning and management of the assigned clinical study/studies end-to-end to achieve objectives. Accountable for proactive, iterat......
The Study Start-Up (SSU) Lead plans and executes global SSU activities to ensure timely trial document and task completion to enable country HA (Health Authorities) and Ethics Committee submissions and site activation to meet ambitious recruitment plans. The Study Start-Up Lead works collaboratively......
Hiring In Warsaw, Poland
full-time Sourced
OND 6-yearsIQVIA Hol...ScraperLoicx
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to manage phase II-III clinical research projects in different therapeutic areas and......
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to work with one single client and to manage clinical research projects in different......
Hiring In Istanbul, Turkey
full-time Sourced
OND 5-yearsIQVIA Hol...ScraperLoicx
The Project Oversight Lead provides direct oversight, support, and coordination for assigned programs and projects within the department to ensure that all assigned Sponsor activities/tasks are worked on and/or escalated per Sponsor procedures. The service will proactively communicate to Sponsor t......
Hiring In Reading, Berkshire, United Kingdom
full-time Sourced
General 6-yearsIQVIA Hol...ScraperLoicx
Location: Remote, candidates must be based in the US Join IQVIA’s 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 outco......
Hiring In Durham, North Carolina, United States of Ame......
full-time Sourced
OND GeneralIQVIA Hol...ScraperLoicx
Location: Remote, candidates must be based in the US Join IQVIA’s 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 outco......
Hiring In Durham, North Carolina, United States of Ame......
full-time Sourced
OND GeneralIQVIA Hol...ScraperLoicx