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......
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......
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
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 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......
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......
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 meet contractual......
Hiring In Seoul, Republic of Korea
full-time Sourced
OND 6-yearsIQVIA Hol...ScraperLoicx
The flex resource performing the Program Delivery Management, IP services will be responsible for the oversight and the training strategy/delivery of Investigational Product (IP) across relevant GCO roles and sites. Activities include engaging with investigational sites as it relates to IP and s......
Are you interested in collaborating with leading pharma companies to help patients all around the world? When you join IQVIA as a sponsor-dedicated Senior CRA in Poland, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with ......
Hiring In Warsaw, Poland
full-time Sourced
General 3-yearsIQVIA 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......
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......
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......
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......
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
Our ever-growing Lifecycle Safety Medical team is expanding. We are hiring Associate Medical Safety Directors in Portugal, Hungary, Slovakia, Romania, Bulgaria, Serbia, Ukraine and Croatia. The role participates in all aspects of the Medical Safety activities as per scope of work. This includes, b......
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 Paris, France
full-time Sourced
OND 5-yearsIQVIA Hol...ScraperLoicx
IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expert......
Hiring In Amsterdam, Netherlands
full-time Sourced
General 3-yearsIQVIA Hol...ScraperLoicx
The IQVIA Sponsor-Dedicated Clinical Trials Assistant Team is supporting the project teams in the execution of clinical trials. Joining the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas. You will be involved ......
Are you interested in collaborating with leading pharma companies to help patients all around the world? When you join IQVIA as a sponsor-dedicated Senior CRA in Poland, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with ......
Hiring In Warsaw, Poland
full-time Sourced
General 3-yearsIQVIA Hol...ScraperLoicx
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......
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......
Senior Epidemiologist, Oncology, Breast Cancer, Real World Evidence - FSP (Sponsor Dedicated) Location: Remote, candidates must be US-based 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 h......
Hiring In Durham, North Carolina, United States of Ame......
full-time Sourced
OND 9-yearsIQVIA Hol...ScraperLoicx
Job Overview Project Management Analysts (PMA) 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 PMA works in partnership with the Project Leader (PL)/Clinical Project Manager (CPM) providing suppo......
Hiring In Seoul, Republic of Korea
full-time Sourced
OND 3-yearsIQVIA 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......
Hiring In Durham, North Carolina, United States of Ame......
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......
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......
Job Overview Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s requirements. Essential Functions • Develop Coordinate the development of investigato......
To be eligible for this position, you must reside in the same country where the job is located. Whether you’re beginning or continuing your career as a CRA, this role is an ideal stepping-stone. You’ll have training and development to plan and progress your career in the direction you choose. And yo......
Hiring In Durham, North Carolina, United States of Ame......
We are seeking an experienced Clinical Research Associate , fully sponsor-dedicated, with a strong background in oncology trials . This is an excellent opportunity to advance your career within a leading global CRO , where you’ll work in a stable, supportive, and international environment that ......
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......
Senior Clinical Research Associate 1 IQVIA is the Human Data Science Company oriented to drive human health outcomes forward. When you join IQVIA Spain 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 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......
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......
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 from start-up through ......
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......
Fonction : Associé(e) de recherche clinique (ARC) principal(e) 2 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 ess......
Assoc. Site Activation Manager - Sponsor Dedicated 
full-time
Sourced
Associate
General
